Congenital familial hypertonia.

about

Congenital familial hypertonia.

Item

http://www.wikidata.org/entity/Q44168700

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh-hant

name

Congenital familial hypertonia.

@en

Congenital familial hypertonia.

@nl

type

Item

label

Congenital familial hypertonia.

@en

Congenital familial hypertonia.

@nl

prefLabel

Congenital familial hypertonia.

@en

Congenital familial hypertonia.

@nl

P1476

Congenital familial hypertonia.

@en

P2093

Carl F DeLuca

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

William J Cashore

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

P2860

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis

P304

529-532

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P31

scholarly article

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10.1177/000992280204100713

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P433

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

P478

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

P577

2002-09-01T00:00:00Z

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

P698

12365318

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

Congenital familial hypertonia.

about

Congenital familial hypertonia.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698