Familiar Meniere's disease restricted to 1.48 Mb on chromosome 12p12.3 by allelic and haplotype association

Journal of Human Genetics

Volumn 55, Issue 12, 2010, Pages 834-837

  Gabriková, Dana ^a,b   Frykholm, Carina ^c   Friberg, Ulla ^c   Lahsaee, Sara ^a   Entesarian, Miriam ^a   Dahl, Niklas ^a   Klar, Joakim ^a  

^a UPPSALA UNIVERSITY   (Sweden)

^b UNIVERSITY OF PRE OV   (Slovakia)

^c UPPSALA UNIVERSITY   (Sweden)

Author keywords

association; chromosome 12; linkage; Meniere's disease

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 12P; CONTROLLED STUDY; FAMILIAL DISEASE; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; HAPLOTYPE; HUMAN; MENIERE DISEASE;

ALLELES; CHROMOSOMES, HUMAN, PAIR 12; GENETIC LINKAGE; HAPLOTYPES; HUMANS; LITHOSTATHINE; MENIERE DISEASE; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC; SWEDEN;

EID: 78650564914     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1038/jhg.2010.122     Document Type: Article

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