학술논문
Autosomal recessive spinocerebellar ataxia type 4 due to a novel homozygous mutation in the VPS13D gene in a Saudi family
Document Type
Article
Author
Source
In: Clinical Neurology and Neurosurgery . (Clinical Neurology and Neurosurgery, May 2024, 240)
Subject
Language
English
ISSN
18726968
03038467
03038467