Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Identifieur interne : 004190 ( Istex/Curation ); précédent : 004189; suivant : 004191Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Auteurs : Shu-Shan Zhang [République populaire de Chine] ; Qin Chen [République populaire de Chine] ; Xue-Ping Chen [République populaire de Chine] ; Jian-Gang Wang [République populaire de Chine] ; Jean-Marc Burgunder [République populaire de Chine] ; Hui-Fang Shang [République populaire de Chine] ; Jean-Marc Burgunder [Suisse] ; Yuan Yang [République populaire de Chine]Source :
- Movement Disorders [ 0885-3185 ] ; 2008-04-30.
Url:
DOI: 10.1002/mds.21942
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ISTEX:01BB3F1C67F786DEBF79210A2EC95D61127C2B48Curation
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Hui-Fang Shang<affiliation><mods:affiliation>E-mail: hfshang@yahoo.com</mods:affiliation>
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<affiliation wicri:level="1"><mods:affiliation>Department of Neurology, West China Hospital, Sichuan University, Chengdu, SiChuan, China</mods:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Department of Neurology, West China Hospital, Sichuan University, Chengdu, SiChuan</wicri:regionArea>
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Le document en format XML
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