Genetic basis of familial Meniere's disease

Journal of Otolaryngology

Volumn 31, Issue 1, 2002, Pages 1-4

  Fung, Kevin ^a   Xie, Y ^a   Hall, Stephen F ^a   Lillicrap, David P ^a   Taylor, Sherryl A M ^a  

^a QUEEN S UNIVERSITY   (Canada)

Author keywords

Familial; Genetics; Human leukocyte antigen; Meniere's disease; Trinucleotide expansion

Indexed keywords

DNA MARKER; HLA ANTIGEN;

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 6P; CLINICAL ARTICLE; FAMILIAL DISEASE; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HUMAN CELL; MENIERE DISEASE; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

EID: 0036203643     PISSN: 03816605     EISSN: None     Source Type: Journal    
DOI: 10.2310/7070.2002.19261     Document Type: Article

References (14)

1. Meniere's syndrome
2. Familial Meniere's disease: A genetic investigation
3. Anticipation in Meniere's disease
4. HLA associates with Meniere's disease
5. Meniere's disease as an autosomal dominant hereditary disease
6. Further observations on the role of the MHC genes and certain hearing disorders
7. A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies
8. HLA antigens in the pathogenesis of Meniere's disease
9. On genetic and environmental factors in Meniere's disease
10. Immune-complex-associated deafness: Preliminary communication
11. Etiopathogenesis of otosclerosis: A hypothesis
12. Meniere's disease and fibrositis syndrome (psychogenic rheumatism). Relationship in audiometric and nystagmographic results
13. Incidence and clinical relevance of antibodies to phospholipid, serotonin and ganglioside in patients with sudden deafness and progressive inner ear hearing loss
14. Otoneurologic and audiologic findings in fibromyalgia