Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26

European Journal of Human Genetics

Volumn 9, Issue 9, 2001, Pages 667-671

  Mangino, Massimo ^a   Flex, Elisabetta ^a   Capon, Francesca ^b   Sangiuolo, Federica ^b   Carraro, Edoardo ^c   Gualandi, Francesca ^c   Mazzoli, Manuela ^c   Martini, Alessandro ^c   Novelli, Giuseppe ^b   Dallapiccola, Bruno ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b UNIVERSITY OF ROME TOR VERGATA   (Italy)

^c UNIVERSITY OF FERRARA   (Italy)

Author keywords

15q25 26; DFNA30; Genetic linkage; Nonsyndromic hearing impairment

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 15Q; CHROMOSOME MAP; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILY; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC ANALYSIS; HAPLOTYPE; HEARING IMPAIRMENT; HUMAN; ITALY; MALE; MARKER GENE; NONSYNDROMIC HEARING IMPAIRMENT; OTOSCLEROSIS; PRIORITY JOURNAL; SENSORY DYSFUNCTION;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; PEDIGREE;

EID: 0034809031     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200707     Document Type: Article

References (24)

1. Epidemiology, etiology and genetic patterns
2. Genomics and hearing impairment
3. Nonsyndromic hearing impairment: Unparalleled heterogeneity
4. A genetic approach to understanding auditory function
5. Two deaf mice, two deaf mice: Murine candidate genes pinpoint the genetic bases of non-syndromic hearing loss in humans
6. Easy calculations of lod scores and genetic risks on small computers
7. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13
8. Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15
9. Localization of a gene for otosclerosis to chromosome 15q25-q26
10. A comprehensive genetic map of the human genome based on 5,264 microsatellites
11. A second-generation linkage map of the human genome
12. The 1993-94 Genethon human genetic linkage map
13. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
14. Structure of the human aggrecan gene: Exon-intron organization and association with the protein domains
15. A human-specific polymorphism in the coding region of the aggrecan gene. Variable number of tandem repeats produce a range of core protein sizes in the general population
16. A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22
17. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
18. Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
19. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
20. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
21. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
22. Non-syndromal autosomal dominant hearing impairment: Ongoing phenotypical characterization of genotypes
23. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24
24. Dominant modifier DFNM1 suppresses recessive deafness DFNB26