MovDisordV3, Main, Exploration, bibRecord, 000277

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

Identifieur interne : 000277 ( Main/Exploration ); précédent : 000276; suivant : 000278

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

Auteurs : Zhong-Bin Zhang [République populaire de Chine] ; Mao-Qiang Tian [République populaire de Chine] ; Kai Gao [République populaire de Chine] ; Yu-Wu Jiang [République populaire de Chine] ; Ye Wu [République populaire de Chine]

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.

RBID : pubmed:26195193
DOI: 10.1002/mds.26216
PubMed: 26195193

Affiliations:

Le document en format XML

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Movement Disorders (revue)

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

De novo KCNMA1 mutations in children with early-onset paroxysmal dyskinesia and developmental delay.

Source :

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Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

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	Movement Disorders (revue)
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