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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13).
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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13).
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). PLoS One. 2011 Mar 29; 6(3):e17811.
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PubMed
subject areas
Adolescent
Amino Acid Substitution
Animals
Base Sequence
DNA
DNA Mutational Analysis
Humans
Kinetics
Magnetic Resonance Imaging
Middle Aged
Molecular Sequence Data
Mutation
Oocytes
Phenotype
Shaw Potassium Channels
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Xenopus laevis
authors with profiles
Christopher M. Gomez