Spinocerebellar ataxia 14 : Novel mutation in exon 2 of PRKCG in a German family
Identifieur interne : 004046 ( Main/Merge ); précédent : 004045; suivant : 004047Spinocerebellar ataxia 14 : Novel mutation in exon 2 of PRKCG in a German family
Auteurs : Dagmar Nolte [Allemagne] ; Melanie Landendinger [Allemagne] ; Eberhard Schmitt [Allemagne] ; Ulrich Müller [Allemagne]Source :
- Movement disorders [ 0885-3185 ] ; 2007.
Descripteurs français
- Pascal (Inist)
English descriptors
Abstract
We describe a novel mutation in the gene coding for protein kinase C gamma (PRKCG) in patients of a German family affected with slowly progressive gait ataxia, dysarthria, and nystagmus. The G/T missense mutation occurred in exon 2 of PRKCG and results in a substitution of glycine by valine (G63V) in the evolutionarily highly conserved cysteine-rich region 1/C1 domain of PRKCG. Among the 20 mutations described to date, this is the first mutation located in exon 2 of PRKCG.
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Pascal:07-0133258Le document en format XML
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<series><title level="j" type="main">Movement disorders</title>
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<term>Protein kinase C</term>
<term>Spinocerebellar ataxia</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Ataxie spinocérébelleuse</term>
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<front><div type="abstract" xml:lang="en">We describe a novel mutation in the gene coding for protein kinase C gamma (PRKCG) in patients of a German family affected with slowly progressive gait ataxia, dysarthria, and nystagmus. The G/T missense mutation occurred in exon 2 of PRKCG and results in a substitution of glycine by valine (G63V) in the evolutionarily highly conserved cysteine-rich region 1/C1 domain of PRKCG. Among the 20 mutations described to date, this is the first mutation located in exon 2 of PRKCG.</div>
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