Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Identifieur interne : 004190 ( Istex/Corpus ); précédent : 004189; suivant : 004191Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Auteurs : Shu-Shan Zhang ; Qin Chen ; Xue-Ping Chen ; Jian-Gang Wang ; Jean-Marc Burgunder ; Hui-Fang Shang ; Jean-Marc Burgunder ; Yuan YangSource :
- Movement Disorders [ 0885-3185 ] ; 2008-04-30.
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DOI: 10.1002/mds.21942
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ISTEX:01BB3F1C67F786DEBF79210A2EC95D61127C2B48Le document en format XML
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