A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Author:

Campbell D A,McHale D P,Brown K A,Moynihan L M,Houseman M,Karbani G,Parry G,Janjua A H,Newton V,al-Gazali L,Markham A F,Lench N J,Mueller R F

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Genes responsible for human hereditary deafness: symphony of a thousand;Petit, C.;Nat Genet,1996

2. Nonsyndromic hearing impairment: unparalleled heterogeneity;G, Van Camp; PJ, Willems; RJH, Smith;Am J Hum Genet,1997

3. Linkage of congenital recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population;Baldwin, C.; Weiss, S.; Farrer, L.;Hum Mol Genet,1995

4. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q;Fukushima, K.; Arabandi, R.; Srisailapathy, C.;Hum Mol Genet,1995

5. An autosomal recessive non-syndromic form of sensorineural hearing loss maps to 3p-DFNB6;Fukushima, K.; Ramesh, A.; Srisailapathy, C.R.;Genome Res,1995

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