A De Novo Missense NPTX1 Variant in an Individual with Infantile‐Onset Cerebellar Ataxia
- Resource Type
- Source
- Movement Disorders. 37:1774-1776
- Subject
Cerebellar Ataxia Neurology Mutation Mutation, Missense Humans Neurology (clinical) Pedigree - Language
- ISSN
- 1531-8257
0885-3185