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 : 001821Novel 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.
Url:
DOI: 10.1002/mds.21093
Affiliations:
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ISTEX:C269B5A1829298DD9191791691D7D3AFF7133999Le document en format XML
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