MovDisordV3, Main, Exploration, bibRecord, 002F51

Codon 101 of PRKCG, a preferential mutation site in SCA14

Identifieur interne : 002F51 ( Main/Exploration ); précédent : 002F50; suivant : 002F52

Codon 101 of PRKCG, a preferential mutation site in SCA14

Auteurs : Dagmar Nolte [Allemagne] ; Stephan Klebe [Allemagne] ; Ralf Baron [Allemagne] ; Günther Deuschl [Allemagne] ; Ulrich Müller [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2007-09-15.

RBID : ISTEX:315ED421D80214D4473E5943562A77E5732662DE

English descriptors

KwdEn :
- Codon (genetics), DNA Mutational Analysis, Exons (genetics), Family Health, Histidine (genetics), Humans, Male, Middle Aged, Mutation, Protein Kinase C (genetics), Spinocerebellar Ataxias (classification), Spinocerebellar Ataxias (genetics), Tyrosine (genetics).
MESH :
- chemical , genetics : Codon, Histidine, Protein Kinase C, Tyrosine.
- classification : Spinocerebellar Ataxias.
- genetics : Exons, Spinocerebellar Ataxias.
- DNA Mutational Analysis, Family Health, Humans, Male, Middle Aged, Mutation.

Url:

https://api.istex.fr/document/315ED421D80214D4473E5943562A77E5732662DE/fulltext/pdf

DOI: 10.1002/mds.21654

Affiliations:

Le document en format XML

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<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Protein Kinase C (genetics)</term>
<term>Spinocerebellar Ataxias (classification)</term>
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<term>Spinocerebellar Ataxias</term>
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Movement Disorders (revue)

Codon 101 of PRKCG, a preferential mutation site in SCA14

Codon 101 of PRKCG, a preferential mutation site in SCA14

Source :

English descriptors

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

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	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.