ArticleBrain : a journal of neurology2020

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.

Ilse Eidhof et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.