Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Identifieur interne : 002553 ( Main/Curation ); précédent : 002552; suivant : 002554Two 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.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Proteins.
- genetics : Gait Disorders, Neurologic, Spastic Paraplegia, Hereditary.
- pathology : Corpus Callosum, Spastic Paraplegia, Hereditary.
- Adult, Consanguinity, Female, Humans, Magnetic Resonance Imaging, Male, Mutation.
Url:
DOI: 10.1002/mds.21942
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ISTEX:01BB3F1C67F786DEBF79210A2EC95D61127C2B48Curation
No country items
Hui-Fang Shang<affiliation><wicri:noCountry code="no comma">E-mail: hfshang@yahoo.com</wicri:noCountry>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Department of Neurology, West China Hospital, Sichuan University, Chengdu, SiChuan</wicri:regionArea>
<wicri:noRegion>SiChuan</wicri:noRegion>
</affiliation>
Le document en format XML
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<series><title level="j">Movement Disorders</title>
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<term>Gait Disorders, Neurologic (genetics)</term>
<term>Humans</term>
<term>Magnetic Resonance Imaging</term>
<term>Male</term>
<term>Mutation</term>
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<term>Spastic Paraplegia, Hereditary (genetics)</term>
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<term>Spastic Paraplegia, Hereditary</term>
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