Codon 101 of PRKCG, a preferential mutation site in SCA14
Identifieur interne : 002F51 ( Main/Exploration ); précédent : 002F50; suivant : 002F52Codon 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.
English descriptors
- KwdEn :
- 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:
DOI: 10.1002/mds.21654
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream Istex, to step Checkpoint: 001A59
- to stream PubMed, to step Corpus: 002579
- to stream PubMed, to step Curation: 002579
- to stream PubMed, to step Checkpoint: 002907
- to stream Ncbi, to step Merge: 001D80
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- to stream Ncbi, to step Checkpoint: 001D80
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- to stream Main, to step Curation: 002F51
Le document en format XML
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<term>Family Health</term>
<term>Histidine (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Protein Kinase C (genetics)</term>
<term>Spinocerebellar Ataxias (classification)</term>
<term>Spinocerebellar Ataxias (genetics)</term>
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<term>Spinocerebellar Ataxias</term>
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<term>Middle Aged</term>
<term>Mutation</term>
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