Polymorphisms in KCNE1 or KCNE3 are not associated with ménière disease in the Caucasian population

American Journal of Medical Genetics, Part A

Volumn 152, Issue 1, 2010, Pages 67-74

  Campbell, Colleen A ^a,b   Della Santina, Charley C ^c,d,e   Meyer, Nicole C ^a   Smith, Nancy B ^c,d,e   Myrie, Oluwaseun A ^c,d,e   Stone, Edwin M ^a,b   Fukushima, Kuni ^f   Califano, Joseph ^c,d,e   Carey, John P ^c,d,e   Hansen, Marlan R ^a   Gantz, Bruce J ^a   Minor, Lloyd B ^c,d,e   Smith, Richard J H ^a,b  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c JOHNS HOPKINS UNIVERSITY   (United States)

^d Johns Hopkins University   (United States)

^e JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f OKAYAMA UNIVERSITY   (Japan)

Author keywords

Association study; KCNE1; KCNE3; M ni re disease; Single nucleotide polymorphism

Indexed keywords

POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNE1; POTASSIUM CHANNEL KCNE3; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CAUCASIAN; CONTROLLED STUDY; ENDOLYMPHATIC SAC; FEMALE; GENE ACTIVITY; GENE EXPRESSION; GENE FREQUENCY; GENETIC ASSOCIATION; GENOTYPE; HOMEOSTASIS; HUMAN; HUMAN CELL; INNER EAR; ION TRANSPORT; JAPANESE; MAJOR CLINICAL STUDY; MALE; MENIERE DISEASE; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; POPULATION GENETICS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STRIA VASCULARIS; TINNITUS; VERTIGO; AMINO ACID SUBSTITUTION; DNA POLYMORPHISM; GENE SEQUENCE; GENETIC SCREENING; HAPLOTYPE MAP; HETEROZYGOSITY; HOMOZYGOSITY; PROTEIN EXPRESSION;

AGED; CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; HUMANS; MALE; MENIERE DISEASE; POLYMORPHISM, SINGLE NUCLEOTIDE; POTASSIUM CHANNELS, VOLTAGE-GATED;

EID: 75149191394     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33114     Document Type: Article

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