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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
00:06

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31

L J Pulleyn1, A P Jackson, E Roberts

  • 1Molecular Medicine Unit, University of Leeds, St James's University Hospital, UK.

European Journal of Human Genetics : EJHG
|February 15, 2001
PubMed

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