Hanein, S., Perrault, I., Roche, O., Gerber, S., Khadom, N., Rio, M., . . . Rozet, J. (2009). TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy. Elsevier.
استشهاد بنمط شيكاغوHanein, Sylvain, et al. TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy. Elsevier, 2009.
MLA استشهادHanein, Sylvain, et al. TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy. Elsevier, 2009.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.