Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among chinese kindreds

International Journal of Neuroscience

Volumn 122, Issue 10, 2012, Pages 560-562

  Jia, Dandan ^a   Tang, Beisha ^a,b,c   Chen, Zhao ^a   Shi, Yuting ^a   Sun, Zhanfang ^a   Zhang, Li ^a   Wang, Junling ^a   Xia, Kun ^b   Jiang, Hong ^a,b,c  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b National Key Lab of Medical Genetics of China Changsha   (China)

^c CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Adca; afg3l2 gene; Mutation analysis; Sca28; Snps

Indexed keywords

PROTEIN; PROTEIN SCA28; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHINA; CHINESE; FEMALE; GENE MUTATION; GENETIC SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; MUTATIONAL ANALYSIS; PROTEIN ANALYSIS; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPINOCEREBELLAR DEGENERATION;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; ATAXIA; ATP-DEPENDENT PROTEASES; CHILD; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; SPINOCEREBELLAR DEGENERATIONS;

EID: 84866419790     PISSN: 00207454     EISSN: 15635279     Source Type: Journal    
DOI: 10.3109/00207454.2012.690796     Document Type: Article

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