KCNA2 mutations are rare in hereditary spastic paraplegia.

about

KCNA2 mutations are rare in hereditary spastic paraplegia.

Item

http://www.wikidata.org/entity/Q48117972

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

KCNA2 mutations are rare in hereditary spastic paraplegia.

@en

KCNA2 mutations are rare in hereditary spastic paraplegia.

@nl

type

Item

label

KCNA2 mutations are rare in hereditary spastic paraplegia.

@en

KCNA2 mutations are rare in hereditary spastic paraplegia.

@nl

prefLabel

KCNA2 mutations are rare in hereditary spastic paraplegia.

@en

KCNA2 mutations are rare in hereditary spastic paraplegia.

@nl

P1476

KCNA2 mutations are rare in hereditary spastic paraplegia.

@en

P2093

Grace Yoon

http://www.w3.org/2001/XMLSchema#string

Oksana Suchowersky

http://www.w3.org/2001/XMLSchema#string

P2860

A new Kv1.2 channelopathy underlying cerebellar ataxia.

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia

P304

325-326

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ANA.24855

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Guy A. Rouleau

Ziv Gan-Or

Nicolas Dupré

P577

2016-12-26T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

28019661

http://www.w3.org/2001/XMLSchema#string