MovDisordV3, Ncbi, Merge, bibRecord, 003082

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.

Identifieur interne : 003082 ( Ncbi/Merge ); précédent : 003081; suivant : 003083

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.

Auteurs : Li Cao ; Qing-Zhou Fei ; Wei-Guo Tang ; Jian-Rong Liu ; Lan Zheng ; Qin Xiao ; Song-Bin He ; Yi Fu ; Sheng-Di Chen

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2011.

RBID : pubmed:21452256

English descriptors

KwdEn :
- Adolescent, Adult, Female, Humans, Male, Mutation, Missense, Pedigree, RNA Splice Sites (genetics), Spastic Paraplegia, Hereditary (genetics), Steroid Hydroxylases (genetics), Young Adult.
MESH :
- chemical , genetics : RNA Splice Sites, Steroid Hydroxylases.
- genetics : Spastic Paraplegia, Hereditary.
- Adolescent, Adult, Female, Humans, Male, Mutation, Missense, Pedigree, Young Adult.

DOI: 10.1002/mds.23466
PubMed: 21452256

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pubmed:21452256

Le document en format XML

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<author><name sortKey="Cao, Li" sort="Cao, Li" uniqKey="Cao L" first="Li" last="Cao">Li Cao</name>
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<author><name sortKey="Fei, Qing Zhou" sort="Fei, Qing Zhou" uniqKey="Fei Q" first="Qing-Zhou" last="Fei">Qing-Zhou Fei</name>
</author>
<author><name sortKey="Tang, Wei Guo" sort="Tang, Wei Guo" uniqKey="Tang W" first="Wei-Guo" last="Tang">Wei-Guo Tang</name>
</author>
<author><name sortKey="Liu, Jian Rong" sort="Liu, Jian Rong" uniqKey="Liu J" first="Jian-Rong" last="Liu">Jian-Rong Liu</name>
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<author><name sortKey="Zheng, Lan" sort="Zheng, Lan" uniqKey="Zheng L" first="Lan" last="Zheng">Lan Zheng</name>
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<author><name sortKey="Xiao, Qin" sort="Xiao, Qin" uniqKey="Xiao Q" first="Qin" last="Xiao">Qin Xiao</name>
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<author><name sortKey="He, Song Bin" sort="He, Song Bin" uniqKey="He S" first="Song-Bin" last="He">Song-Bin He</name>
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<author><name sortKey="Fu, Yi" sort="Fu, Yi" uniqKey="Fu Y" first="Yi" last="Fu">Yi Fu</name>
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<author><name sortKey="Chen, Sheng Di" sort="Chen, Sheng Di" uniqKey="Chen S" first="Sheng-Di" last="Chen">Sheng-Di Chen</name>
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<author><name sortKey="He, Song Bin" sort="He, Song Bin" uniqKey="He S" first="Song-Bin" last="He">Song-Bin He</name>
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<term>Adult</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.</ArticleTitle>
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<name sortKey="Chen, Sheng Di" sort="Chen, Sheng Di" uniqKey="Chen S" first="Sheng-Di" last="Chen">Sheng-Di Chen</name>
<name sortKey="Fei, Qing Zhou" sort="Fei, Qing Zhou" uniqKey="Fei Q" first="Qing-Zhou" last="Fei">Qing-Zhou Fei</name>
<name sortKey="Fu, Yi" sort="Fu, Yi" uniqKey="Fu Y" first="Yi" last="Fu">Yi Fu</name>
<name sortKey="He, Song Bin" sort="He, Song Bin" uniqKey="He S" first="Song-Bin" last="He">Song-Bin He</name>
<name sortKey="Liu, Jian Rong" sort="Liu, Jian Rong" uniqKey="Liu J" first="Jian-Rong" last="Liu">Jian-Rong Liu</name>
<name sortKey="Tang, Wei Guo" sort="Tang, Wei Guo" uniqKey="Tang W" first="Wei-Guo" last="Tang">Wei-Guo Tang</name>
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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.

Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki