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Original Communication - Study of families of nonsyndromic hearing impairment segregating with mutations in Cx26 gene, 12/2004
Autosomal recessive nonsyndromic hearing impairment (ARNSHI) is the most common form with profound hereditary hearing impairment linked to DFNB1 locus... 
Connexin26, W24X mutation, NSHI, India
Journal
European Archives of Oto-Rhino-Laryngology, ISSN 0937-4477, 05/2016, Volume 273, Issue 5, pp. 1161 - 1165
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, p. e0124232
Journal Article
Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 09/2015, Volume 19, Issue 9, pp. 512 - 527
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 2009, Volume 74, Issue 4, pp. 351 - 355
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2019, Volume 27, Issue 6, pp. 869 - 878
Roma are a socially and culturally distinct isolated population with genetically divergent subisolates, residing mainly across Central, Southern, and Eastern... 
SURVIVAL | CYTOARCHITECTURE | POPULATION | GJB2 | W24X MUTATION | MAP3K1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | HEALTH | Calponin | USH2A protein | Preservation | Etiology | Hair cells | Homology | Scaling | Genetic diversity | Hearing impairment | Population genetics | Multidimensional scaling | Hearing loss
Journal Article
Balkan Journal of Medical Genetics, ISSN 1311-0160, 1/2009, Volume 12, Issue 2, pp. 11 - 16
Hearing impairment is a common sensori-neural disorder with the incidence of profound deafness in one per 1,000 births. Non syndromic recessive deafness... 
Connexin 26 | Deafness | Mutations | Non syndromic hearing loss (NSHL) | GJB2 Gene | 35delG | CONNEXIN-26 GJB2 | GENE | FREQUENCY | W24X | GENETICS & HEREDITY | IMPAIRMENT
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 08/2005, Volume 10, Issue 2
Autosomal recessive nonsyndromic hearing impairment (ARNSHI) is the most common form with profound hereditary hearing impairment linked to DFNB1 locus... 
Connexin26 | NSHI | W24X mutation | India
Journal Article
International Journal of Human Genetics, ISSN 0972-3757, 12/2005, Volume 5, Issue 4, pp. 241 - 246
Autosomal Recessive Nonsyndromic Hearing Impairment (ARNSHI) is caused by mutations in the gap junction gene GJB2 or Connexin26 gene (Cx26) in many of the... 
mutation | NSHI | GJB2 | W24X | India
Journal Article
Indian Journal of Human Genetics, ISSN 0971-6866, 07/2004, Volume 10, Issue 2, pp. 58 - 64
Autosomal recessive nonsyndromic hearing impairment (ARNSHI) is the most common form with profound hereditary hearing impairment linked to DFNB1 locus... 
Connexin26 | W24X mutation | NSHI | India | Case studies | Genetic aspects | Research | Gene mutations | Hearing disorders
Journal Article
Journal Article
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