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Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias.SCA23 and prodynorphin: is it time for gene retraction?Reply: SCA23 and prodynorphin: is it time for gene retraction?
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 17 December 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Spinocerebellar ataxia type 23: a genetic update.
@en
Spinocerebellar ataxia type 23: a genetic update.
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type
label
Spinocerebellar ataxia type 23: a genetic update.
@en
Spinocerebellar ataxia type 23: a genetic update.
@nl
prefLabel
Spinocerebellar ataxia type 23: a genetic update.
@en
Spinocerebellar ataxia type 23: a genetic update.
@nl
P2860
P1433
P1476
Spinocerebellar ataxia type 23: a genetic update.
@en
P2093
Dineke S Verbeek
P2860
P2888
P304
P356
10.1007/S12311-008-0085-1
P577
2008-12-17T00:00:00Z