<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1395</year>
	<month>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2017</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>21</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa>The First Report of a 290-bp Deletion in β-Globin  Gene in the South of Iran</title_fa>
	<title>The First Report of a 290-bp Deletion in β-Globin  Gene in the South of Iran</title>
	<subject_fa>Molecular Genetics &amp; Genomics</subject_fa>
	<subject>Molecular Genetics &amp; Genomics</subject>
	<content_type_fa>مقاله کوتاه</content_type_fa>
	<content_type>Short Communication</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p style=&quot;direction: ltr; &quot;&gt;&lt;strong&gt;Background&lt;/strong&gt;: &amp;beta;-thalassemia is one of the most widespread disease in the world, including Iran. In this study, we reported, for the first time, A 290-bp &lt;em&gt;&amp;beta;&lt;/em&gt;-&lt;em&gt;globin&lt;/em&gt; gene deletion in the south of Iran. &lt;strong&gt;Methods:&lt;/strong&gt; Four individuals from three unrelated families with Arabic ethnic background were studied in Khuzestan Province. Red blood cell indices and hemoglobin analysis were carried out according to the standard methods. Genomic DNA was obtained from peripheral blood cells by salting out procedures. &lt;em&gt;&amp;beta;&lt;/em&gt;-&lt;em&gt;globin&lt;/em&gt; gene amplification, multiplex ligation-dependent probe ampliﬁcation (MLPA) and DNA sequencing were performed.&lt;strong&gt; Results:&lt;/strong&gt; The PCR followed by sequencing and MLPA test of the &lt;em&gt;&amp;beta;-globin&lt;/em&gt; gene confirmed the presence of a 290-bp deletion in the heterozygous form, along with -88C&gt;A mutation. All the individuals had elevated hemoglobin A&lt;sub&gt;2&lt;/sub&gt; and normal fetal hemoglobin levels. &amp;nbsp;&lt;strong&gt;Conclusions:&lt;/strong&gt; This mutation causes &amp;beta;&lt;sup&gt;0&lt;/sup&gt;-thalassemia and can be highly useful for prenatal diagnosis in compound heterozygous condition with different &lt;em&gt;&amp;beta;-globin&lt;/em&gt; gene mutations.&lt;/p&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>β-thalassemia, β-globin gene mutation, Iran, Multiplex ligation-dependent probe ampliﬁcation</keyword>
	<start_page>126</start_page>
	<end_page>128</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-1-597&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mohammad</first_name>
	<middle_name></middle_name>
	<last_name>Hamid</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Ladan</first_name>
	<middle_name></middle_name>
	<last_name>Dawoody Nejad</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Gholamreza</first_name>
	<middle_name></middle_name>
	<last_name>Shariati</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>Shariatig@yahoo.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Dept. of Medical  Genetic, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hamid</first_name>
	<middle_name></middle_name>
	<last_name>Galehdari</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Medical  Genetic, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Alihossein</first_name>
	<middle_name></middle_name>
	<last_name>Saberi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Medical  Genetic, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Marziye</first_name>
	<middle_name></middle_name>
	<last_name>Mohammadi-Anaei</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Narges Medical Genetics and Prenatal Diagnosis Laboratory, No. 18, East Mihan Ave., Kianpars, Ahvaz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
