Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families
Open Access
- 15 December 2007
- journal article
- research article
- Published by Springer Science and Business Media LLC in Journal of Human Genetics
- Vol. 53 (2), 101-105
- https://doi.org/10.1007/s10038-007-0209-3
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Tricellulin Is a Tight-Junction Protein Necessary for HearingAmerican Journal of Human Genetics, 2006
- Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cellsThe Journal of cell biology, 2005
- Allegro version 2Nature Genetics, 2005
- Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non‐syndromic hearing impairmentClinical Genetics, 2004
- A Combined Linkage-Physical Map of the Human GenomeAmerican Journal of Human Genetics, 2004
- A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1Human Genetics, 2004
- Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potentialJournal of Cell Science, 2004
- The Colorado Newborn Hearing Screening Project, 1992–1999: On the Threshold of Effective Population-Based Universal Newborn Hearing ScreeningPublished by American Academy of Pediatrics (AAP) ,2002
- Primer3 on the WWW for General Users and for Biologist ProgrammersMethods in molecular biology (Clifton, N.J.), 1999
- Genetic Epidemiology of Hearing ImpairmentAnnals of the New York Academy of Sciences, 1991