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Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations
- Source :
- Iranian Journal of Public Health, Vol 48, Iss 9 (2019), Iranian Journal of Public Health
- Publication Year :
- 2019
- Publisher :
- Tehran University of Medical Sciences, 2019.
-
Abstract
- Background: Autosomal recessive non-syndromic hearing loss (ARNSHL), one of the global public health concerns, is marked by a high degree of genetic heterogeneity. The role of GJB2, as the most common cause of ARNSHL, is only
- Subjects :
- Hearing loss
DFNB loci
Biology
Iran
03 medical and health sciences
Gjb2 gene
symbols.namesake
0302 clinical medicine
Homozygosity mapping
medicine
otorhinolaryngologic diseases
030212 general & internal medicine
Sanger sequencing
Genetics
030505 public health
Genetic heterogeneity
lcsh:Public aspects of medicine
Public Health, Environmental and Occupational Health
lcsh:RA1-1270
Disease gene identification
Autosomal recessive non-syndromic hearing loss (ARNSHL)
Cohort
symbols
Etiology
Original Article
medicine.symptom
0305 other medical science
Non syndromic
Subjects
Details
- Language :
- English
- ISSN :
- 22516093 and 22516085
- Volume :
- 48
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Iranian Journal of Public Health
- Accession number :
- edsair.doi.dedup.....ce721041cb97f5272e870875a223034e