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Matches in SemOpenAlex for { <https://semopenalex.org/work/W1995140345> ?p ?o ?g. }

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• W1995140345 abstract "In the past two years, considerable progress had been made in the mapping and cloning of human deafness genes. Highlights are the chromosomal localization of a least five genes for autosomal forms of non-syndromic deafness and, more recently, the cloning of an X-linked deafness gene, DFN3, and the Usher syndrome type IB gene. This last gene encodes a myosin-like protein and was identified as the human homolog of the mouse shaker-1 gene. The DFN3 gene Brain 4 encodes a POU domain containing transcription factor that is involved in the development of the inner ear." @default.
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• W1995140345 date "1995-06-01" @default.
• W1995140345 modified "2023-09-27" @default.
• W1995140345 title "Mapping and cloning hereditary deafness genes" @default.
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• W1995140345 doi "https://doi.org/10.1016/0959-437x(95)80053-0" @default.
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