High incidence of deafness from three frequent connexin 26 mutations in an isolated community

scientific article published on 01 January 2006

High incidence of deafness from three frequent connexin 26 mutations in an isolated community is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/GTE.2006.10.40
P698PubMed publication ID16545002

P2093author name stringAravinda Chakravarti
Stavit A Shalev
Joël Zlotogora
Saleh Barges
Minerva Carasquillo
Yasir Hujerat
P433issue1
P921main subjectdeafnessQ12133
P304page(s)40-43
P577publication date2006-01-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleHigh incidence of deafness from three frequent connexin 26 mutations in an isolated community
P478volume10

Reverse relations

cites work (P2860)
Q46379359Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect
Q34184437Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment
Q33794457Consanguinity and birth defects in the jerusalem perinatal study cohort
Q36703593Multiple mutations responsible for frequent genetic diseases in isolated populations

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