Literature DB >> 10196710

DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.

L Moynihan1, M Houseman, V Newton, R Mueller, N Lench.   

Abstract

Autosomal recessive non-syndromal deafness is an extremely heterogeneous condition with at least 19 loci (DFNB1-19) already described. We have used autozygosity mapping to localise a further novel locus, DFNB20, to chromosome 11q25-qter in a consanguineous family originating from Pakistan. A region of homozygosity was observed in affected individuals spanning the interval D11S969-qter.

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Year:  1999        PMID： 10196710     DOI： 10.1038/sj.ejhg.5200269

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN： 1018-4813            Impact factor:   4.246


  2 in total

1.  Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

Authors:  Shahid Y Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I Shabbir; S Amer Riazuddin; Shaheen N Khan; Tayyab Husnain; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
Journal:  Hum Genet       Date:  2006-10-26       Impact factor: 4.132

2.  A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.

Authors:  Arunima Chatterjee; Rajeev Jalvi; Nishtha Pandey; R Rangasayee; Anuranjan Anand
Journal:  Hum Genet       Date:  2008-11-22       Impact factor: 4.132
  2 in total

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