[A novel variation in ATP1A3 gene in a child with CAPOS syndrome].

Subjects

Subjects :

Child
Humans
Mutation
Cerebellar Ataxia genetics
Foot Deformities, Congenital genetics
Hearing Loss, Sensorineural genetics
Optic Atrophy genetics
Reflex, Abnormal genetics
Sodium-Potassium-Exchanging ATPase genetics

Details

Language :

Chinese

ISSN :

0578-1310

Volume :

58

Issue :

3

Database :

MEDLINE

Journal :

Zhonghua er ke za zhi = Chinese journal of pediatrics

Publication Type :

Academic Journal

Accession number :

32135597

Full Text :

https://doi.org/10.3760/cma.j.issn.0578-1310.2020.03.014