Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings

Genetics in Medicine

Volumn 13, Issue 5, 2011, Pages 415-420

  Hietikko, Elina ^a   Kotimäki, Jouko ^b   Kentala, Erna ^c   Klockars, Tuomas ^c   Sorri, Martti ^a   Männikkö, Minna ^a  

^a UNIVERSITY OF OULU   (Finland)

^b KAINUU CENTRAL HOSPITAL   (Finland)

^c UNIVERSITY OF HELSINKI   (Finland)

Author keywords

anticipation; autosomal dominant inheritance; familial; linkage analysis; Meniere disease

Indexed keywords

ADULT; ANTICIPATION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 12P; CONTROLLED STUDY; DISEASE SEVERITY; FAMILIAL DISEASE; FEMALE; FINLAND; GENE LOCUS; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; MENIERE DISEASE; MICROSATELLITE MARKER; MIGRAINE; PENETRANCE; QUESTIONNAIRE; SCORING SYSTEM;

ADULT; AGE OF ONSET; ANTICIPATION, GENETIC; CHROMOSOMES, HUMAN, PAIR 12; FEMALE; FINLAND; GENETIC HETEROGENEITY; HUMANS; LOD SCORE; MALE; MENIERE DISEASE; MIDDLE AGED; MIGRAINE DISORDERS; PEDIGREE; YOUNG ADULT;

EID: 79955897567     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e3182091a41     Document Type: Article

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