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Volumn 14, Issue 3-4, 2013, Pages 257-258

Erratum to: The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together [Neurogenetics, 14, 3-4, 2013 (257-258), DOI 10.1007/s10048-013-0370-0];The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

(10) Duarri, Anna a Nibbeling, Esther a Fokkens, Michiel R a Meijer, Michel a Boddeke, Erik a Lagrange, Emmeline b Stevanin, Giovanni c,d,e,f Brice, Alexis c,d,e,f Durr, Alexandra c,d,e,f Verbeek, Dineke S a

a UNIVERSITY MEDICAL CENTER GRONINGEN (Netherlands)

b GRENOBLE UNIVERSITY HOSPITAL (France)

c INSERM (France)

d SORBONNE UNIVERSITÉ (France)

e CNRS (France)

f PITIÉ SALPÊTRIÈRE HOSPITAL (France)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KV4.3; UNCLASSIFIED DRUG;

ALLELE; BRUGADA SYNDROME; CLINICAL FEATURE; EUROPE; GAIN OF FUNCTION MUTATION; GENE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; HUMAN; KCND3 GENE; LETTER; LOSS OF FUNCTION MUTATION; MORBIDITY; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION;

ADULT; BRUGADA SYNDROME; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; SHAL POTASSIUM CHANNELS; SPINOCEREBELLAR ATAXIAS;

EID: 84888059592 PISSN: 13646745 EISSN: 13646753 Source Type: Journal
DOI: 10.1007/s10048-015-0447-z Document Type: Erratum

Times cited : (16)

References (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.