MovDisordV3, Ncbi, Merge, bibRecord, 002075

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

Identifieur interne : 002075 ( Ncbi/Merge ); précédent : 002074; suivant : 002076

Two 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 Yang

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2008.

RBID : pubmed:18361476

English descriptors

KwdEn :
- Adult, Consanguinity, Corpus Callosum (pathology), Female, Gait Disorders, Neurologic (genetics), Humans, Magnetic Resonance Imaging, Male, Mutation, Proteins (genetics), Spastic Paraplegia, Hereditary (genetics), Spastic Paraplegia, Hereditary (pathology).
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.

DOI: 10.1002/mds.21942
PubMed: 18361476

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

to stream PubMed, to step Corpus: 002286
to stream PubMed, to step Curation: 002286
to stream PubMed, to step Checkpoint: 002010

Links to Exploration step

pubmed:18361476

Le document en format XML

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<author><name sortKey="Chen, Qin" sort="Chen, Qin" uniqKey="Chen Q" first="Qin" last="Chen">Qin Chen</name>
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<author><name sortKey="Chen, Xue Ping" sort="Chen, Xue Ping" uniqKey="Chen X" first="Xue-Ping" last="Chen">Xue-Ping Chen</name>
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<author><name sortKey="Wang, Jian Gang" sort="Wang, Jian Gang" uniqKey="Wang J" first="Jian-Gang" last="Wang">Jian-Gang Wang</name>
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<author><name sortKey="Burgunder, Jean Marc" sort="Burgunder, Jean Marc" uniqKey="Burgunder J" first="Jean-Marc" last="Burgunder">Jean-Marc Burgunder</name>
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<author><name sortKey="Shang, Hui Fang" sort="Shang, Hui Fang" uniqKey="Shang H" first="Hui-Fang" last="Shang">Hui-Fang Shang</name>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Proteins</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.</ArticleTitle>
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<tree><noCountry><name sortKey="Burgunder, Jean Marc" sort="Burgunder, Jean Marc" uniqKey="Burgunder J" first="Jean-Marc" last="Burgunder">Jean-Marc Burgunder</name>
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<name sortKey="Chen, Qin" sort="Chen, Qin" uniqKey="Chen Q" first="Qin" last="Chen">Qin Chen</name>
<name sortKey="Chen, Xue Ping" sort="Chen, Xue Ping" uniqKey="Chen X" first="Xue-Ping" last="Chen">Xue-Ping Chen</name>
<name sortKey="Shang, Hui Fang" sort="Shang, Hui Fang" uniqKey="Shang H" first="Hui-Fang" last="Shang">Hui-Fang Shang</name>
<name sortKey="Wang, Jian Gang" sort="Wang, Jian Gang" uniqKey="Wang J" first="Jian-Gang" last="Wang">Jian-Gang Wang</name>
<name sortKey="Yang, Yuan" sort="Yang, Yuan" uniqKey="Yang Y" first="Yuan" last="Yang">Yuan Yang</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)

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.

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