Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19

Spinocerebellar ataxia type 19 (SCA19), allelic with spinocerebellar ataxia type 22 (SCA22), is a rare syndrome caused by mutations in the KCND3 gene which encodes the potassium channel Kv4.3. Only 18 SCA19/22 families and sporadic cases of different ethnic backgrounds have been previously reported....

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Bibliografiske detaljer
Udgivet i:Cerebellum
Main Authors: Paucar, Martin, Bergendal, Åsa, Gustavsson, Peter, Nordenskjöld, Magnus, Laffita-Mesa, José, Savitcheva, Irina, Svenningsson, Per
Format: Artigo
Sprog:Inglês
Udgivet: Springer US 2018
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Original Paper
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6028832/
https://ncbi.nlm.nih.gov/pubmed/29527639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12311-018-0927-4
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