Tariq, H., Imran, R., & Naz, S. (2018). A Novel Homozygous Variant of SETX Causes Ataxia with Oculomotor Apraxia Type 2. J Clin Neurol.
Citação norma ChicagoTariq, Huma, Rashid Imran, and Sadaf Naz. "A Novel Homozygous Variant of SETX Causes Ataxia With Oculomotor Apraxia Type 2." J Clin Neurol 2018.
ציטוט MLATariq, Huma, Rashid Imran, and Sadaf Naz. "A Novel Homozygous Variant of SETX Causes Ataxia With Oculomotor Apraxia Type 2." J Clin Neurol 2018.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.