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Gene Review:

DFNB44 - deafness, autosomal recessive 44

Homo sapiens

Ansar, M. et al.

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Disease relevance of DFNB44

DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22 [1].

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].

References

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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