MovDisordV3, Main, Exploration, bibRecord, 000353

A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.

Identifieur interne : 000353 ( Main/Exploration ); précédent : 000352; suivant : 000354

A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.

Auteurs : Diane Doummar [France] ; Cyril Mignot [France] ; Emmanuelle Apartis [France] ; Laurent Villard [France] ; Diana Rodriguez [France] ; Sandra Chantot-Bastauraud [France] ; Lydie Burglen [France]

Source :

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

RBID : pubmed:26207815
DOI: 10.1002/mds.26303
PubMed: 26207815

Affiliations:

Le document en format XML

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<author><name sortKey="Chantot Bastauraud, Sandra" sort="Chantot Bastauraud, Sandra" uniqKey="Chantot Bastauraud S" first="Sandra" last="Chantot-Bastauraud">Sandra Chantot-Bastauraud</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.</title>
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Movement Disorders (revue)

A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.

A Novel Homozygous TBC1D24 Mutation Causing Multifocal Myoclonus With Cerebellar Involvement.

Source :

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	Movement Disorders (revue)
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