Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia
Identifieur interne : 001511 ( Main/Curation ); précédent : 001510; suivant : 001512Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia
Auteurs : Li Cao [République populaire de Chine] ; Qing-Zhou Fei [République populaire de Chine] ; Wei-Guo Tang ; Jian-Rong Liu [République populaire de Chine] ; Lan Zheng [République populaire de Chine] ; Qin Xiao [République populaire de Chine] ; Song-Bin He ; Yi Fu [République populaire de Chine] ; Sheng-Di Chen [République populaire de Chine]Source :
- Movement Disorders [ 0885-3185 ] ; 2011-06.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : RNA Splice Sites, Steroid Hydroxylases.
- genetics : Spastic Paraplegia, Hereditary.
- Adolescent, Adult, Female, Humans, Male, Mutation, Missense, Pedigree, Young Adult.
Url:
DOI: 10.1002/mds.23466
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ISTEX:86C9CE7849321A71619AA0B9F51BDCC4408DD59DCuration
No country items
Wei-Guo Tang<affiliation><wicri:noCountry code="subField">China; and</wicri:noCountry>
</affiliation>
<affiliation><wicri:noCountry code="subField">China; and</wicri:noCountry>
</affiliation>
Le document en format XML
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