MovDisordV3, Istex, Checkpoint, bibRecord, 001820

Novel SGCE gene mutation in a Korean patient with myoclonus–dystonia with unique phenotype mimicking Moya–Moya disease

Identifieur interne : 001820 ( Istex/Checkpoint ); précédent : 001819; suivant : 001821

Novel SGCE gene mutation in a Korean patient with myoclonus–dystonia with unique phenotype mimicking Moya–Moya disease

Auteurs : Eun Joo Chung [Corée du Sud] ; Won Yong Lee [Corée du Sud] ; Ji-Youn Kim [Corée du Sud] ; Jong-Hun Kim [Corée du Sud] ; Gyeong-Moon Kim [Corée du Sud] ; Chang Seok Ki [Corée du Sud] ; In-Suk Kim [Corée du Sud]

Source :

Movement Disorders [ 0885-3185 ] ; 2007-06-15.

RBID : ISTEX:C269B5A1829298DD9191791691D7D3AFF7133999
Url:

https://api.istex.fr/document/C269B5A1829298DD9191791691D7D3AFF7133999/fulltext/pdf

DOI: 10.1002/mds.21093

Affiliations:

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ISTEX:C269B5A1829298DD9191791691D7D3AFF7133999

Le document en format XML

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<author><name sortKey="Chung, Eun Joo" sort="Chung, Eun Joo" uniqKey="Chung E" first="Eun Joo" last="Chung">Eun Joo Chung</name>
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<author><name sortKey="Lee, Won Yong" sort="Lee, Won Yong" uniqKey="Lee W" first="Won Yong" last="Lee">Won Yong Lee</name>
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<author><name sortKey="Kim, Ji Oun" sort="Kim, Ji Oun" uniqKey="Kim J" first="Ji-Youn" last="Kim">Ji-Youn Kim</name>
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<author><name sortKey="Kim, Jong Un" sort="Kim, Jong Un" uniqKey="Kim J" first="Jong-Hun" last="Kim">Jong-Hun Kim</name>
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<author><name sortKey="Kim, Gyeong Oon" sort="Kim, Gyeong Oon" uniqKey="Kim G" first="Gyeong-Moon" last="Kim">Gyeong-Moon Kim</name>
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<author><name sortKey="Ki, Chang Seok" sort="Ki, Chang Seok" uniqKey="Ki C" first="Chang Seok" last="Ki">Chang Seok Ki</name>
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<author><name sortKey="Kim, In Uk" sort="Kim, In Uk" uniqKey="Kim I" first="In-Suk" last="Kim">In-Suk Kim</name>
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<author><name sortKey="Kim, In Uk" sort="Kim, In Uk" uniqKey="Kim I" first="In-Suk" last="Kim">In-Suk Kim</name>
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<series><title level="j">Movement Disorders</title>
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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Novel SGCE gene mutation in a Korean patient with myoclonus–dystonia with unique phenotype mimicking Moya–Moya disease

Novel SGCE gene mutation in a Korean patient with myoclonus–dystonia with unique phenotype mimicking Moya–Moya disease

Source :

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri