A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease

Nouri, N., Nouri, N., Aryani, O., Kamalidehghan, B., Sedghi, M. & Houshmand, M. (2012). A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease. Iranian Biomedical Journal, 16(4), 223-225. https://doi.org/10.6091/ibj.1077.2012

Nouri, N., Nouri, N., Aryani, O., Kamalidehghan, B., Sedghi, M., & Houshmand, M. "A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease", Iranian Biomedical Journal, 16, 4, 2012, 223-225. doi: 10.6091/ibj.1077.2012

Nouri N., Nouri N., Aryani O., Kamalidehghan B., Sedghi M., Houshmand M. (2012). 'A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease', Iranian Biomedical Journal, 16(4), pp. 223-225. doi: 10.6091/ibj.1077.2012

N. Nouri, N. Nouri, O. Aryani, B. Kamalidehghan, M. Sedghi & M. Houshmand, "A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease," Iranian Biomedical Journal, 16 4 (2012): 223-225, doi: 10.6091/ibj.1077.2012

Nouri N., Nouri N., Aryani O., Kamalidehghan B., Sedghi M., Houshmand M. A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia with Oculomotor Apraxia Type 1(AOA1) Disease. Iranian Biomedical Journal. 2012;16(4):223-225. doi: 10.6091/ibj.1077.2012