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Gene Review

DFNB44  -  deafness, autosomal recessive 44

Homo sapiens

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Disease relevance of DFNB44


High impact information on DFNB44

  • A novel autosomal recessive NSHI locus, DFNB44, was mapped to a 20.9 cM genetic interval on chromosome 7p14.1-q11.22, according to the Marshfield genetic map, in a consanguineous Pakistani family [1].


  1. DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22. Ansar, M., Chahrour, M.H., Amin Ud Din, M., Arshad, M., Haque, S., Pham, T.L., Yan, K., Ahmad, W., Leal, S.M. Hum. Hered. (2004) [Pubmed]
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