Tariq, H., Imran, R., & Naz, S. (2018). A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2. J Clin Neurol.
استشهاد بنمط شيكاغوTariq, Huma, Rashid Imran, و Sadaf Naz. "A Novel Homozygous Variant of SETX Causes Ataxia With Oculomotor Apraxia Type 2." J Clin Neurol 2018.
MLA استشهادTariq, Huma, Rashid Imran, و Sadaf Naz. "A Novel Homozygous Variant of SETX Causes Ataxia With Oculomotor Apraxia Type 2." J Clin Neurol 2018.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.