Codon 101 of PRKCG, a preferential mutation site in SCA14.
Identifieur interne : 001D80 ( Ncbi/Curation ); précédent : 001D79; suivant : 001D81Codon 101 of PRKCG, a preferential mutation site in SCA14.
Auteurs : Dagmar Nolte ; Stephan Klebe ; Ralf Baron ; Günther Deuschl ; Ulrich MüllerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2007.
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.
DOI: 10.1002/mds.21654
PubMed: 17659643
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