A novel c.3636-4 A>G mutation in the CCDC88C plays a causative role in familial spinocerebellar ataxia

Published 2023 View Full Article

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Title
A novel c.3636-4 A>G mutation in the CCDC88C plays a causative role in familial spinocerebellar ataxia
Authors
Keywords
-
Journal
HUMAN HEREDITY
Volume -, Issue -, Pages -
Publisher
S. Karger AG
Online
2023-10-28
DOI
10.1159/000534692

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