Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
Identifieur interne : 002553 ( Main/Exploration ); 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
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 004190
- to stream Istex, to step Curation: 004190
- to stream Istex, to step Checkpoint: 001109
- to stream PubMed, to step Corpus: 002286
- to stream PubMed, to step Curation: 002286
- to stream PubMed, to step Checkpoint: 002010
- to stream Ncbi, to step Merge: 002075
- to stream Ncbi, to step Curation: 002075
- to stream Ncbi, to step Checkpoint: 002075
- to stream Main, to step Merge: 003131
- to stream Main, to step Curation: 002553
Le document en format XML
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