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. Pasteur Institute of Iran.

Nouri, Nayereh, Narges Nouri, Omid Aryani, Behnam Kamalidehghan, Maryam Sedghi, and Massoud Houshmand. A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia With Oculomotor Apraxia Type 1(AOA1) Disease. Pasteur Institute of Iran, 2012.

Nouri, Nayereh, et al. A Novel Mutation in the Aprataxin (APTX) Gene in an Iranian Individual Suffering Early-Onset Ataxia With Oculomotor Apraxia Type 1(AOA1) Disease. Pasteur Institute of Iran, 2012.