Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.
about
Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia casesCerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias.Plasma membrane poration by opioid neuropeptides: a possible mechanism of pathological signal transduction.Opioid precursor protein isoform is targeted to the cell nuclei in the human brain.SCA23 and prodynorphin: is it time for gene retraction?Reply: SCA23 and prodynorphin: is it time for gene retraction?Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
P2860
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P2860
Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
Identification and characteriz ...... inant cerebellar ataxia cases.
@en
Identification and characteriz ...... inant cerebellar ataxia cases.
@nl
type
label
Identification and characteriz ...... inant cerebellar ataxia cases.
@en
Identification and characteriz ...... inant cerebellar ataxia cases.
@nl
prefLabel
Identification and characteriz ...... inant cerebellar ataxia cases.
@en
Identification and characteriz ...... inant cerebellar ataxia cases.
@nl
P2093
P2860
P50
P1433
P1476
Identification and characteriz ...... inant cerebellar ataxia cases.
@en
P2093
Christophe Robin
Dineke S Verbeek
Fabien Zagnoli
Hiroyuki Watanabe
Jean-Yves Goas
Justyna Jezierska
Jérôme Kok
Michiel R Fokkens
Pierre Bertrand
P2860
P2888
P304
P356
10.1007/S00415-013-6882-6
P577
2013-03-08T00:00:00Z