Spinocerebellar ataxia type 13 is an uncommon SCA subtype in the Chinese Han population

International Journal of Neuroscience

Volumn 123, Issue 7, 2013, Pages 450-453

  Peng, Lan ^a   Wang, Chunrong ^a   Chen, Zhao ^a   Wang, Jun Ling ^a   Tang, Bei Sha ^a,b,c   Jiang, Hong ^a,b  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b Neurodegenerative Disorders Research Center   (China)

^c CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

DHPLC; KCNC3 gene; Mutation analysis; SCA13; Spinocerebellar ataxias

Indexed keywords

KCNC3 PROTEIN; SHAW POTASSIUM CHANNEL; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA SEQUENCE; ELUTION; FEMALE; GENE MUTATION; GENETIC CODE; HEREDITARY ATAXIA; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; MUTATIONAL ANALYSIS; POPULATION RESEARCH; RARE DISEASE; SCHOOL CHILD; SPINOCEREBELLAR ATAXIA TYPE 13; SPINOCEREBELLAR DEGENERATION;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHINA; ETHNIC GROUPS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; SHAW POTASSIUM CHANNELS; SPINOCEREBELLAR ATAXIAS;

EID: 84879177247     PISSN: 00207454     EISSN: 15635279     Source Type: Journal    
DOI: 10.3109/00207454.2013.763254     Document Type: Article

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