APA aipamena

Eidhof, I., Baets, J., Kamsteeg, E., Schenck, A., & van de Warrenburg, B. P. (2020). Reply: A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia; and Novel GDAP2 pathogenic variants cause autosomal recessive spinocerebellar ataxia-27 (SCAR27) in a Chinese family. Brain.

Chicago Style aipamena

Eidhof, Ilse, Jonathan Baets, Erik-Jan Kamsteeg, Annette Schenck, and Bart P. van de Warrenburg. "Reply: A Homozygous GDAP2 Loss-of-function Variant in a Patient With Adult-onset Cerebellar Ataxia; and Novel GDAP2 Pathogenic Variants Cause Autosomal Recessive Spinocerebellar Ataxia-27 (SCAR27) in a Chinese Family." Brain 2020.

MLA aipamena

Eidhof, Ilse, et al. "Reply: A Homozygous GDAP2 Loss-of-function Variant in a Patient With Adult-onset Cerebellar Ataxia; and Novel GDAP2 Pathogenic Variants Cause Autosomal Recessive Spinocerebellar Ataxia-27 (SCAR27) in a Chinese Family." Brain 2020.