Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment

Overview of attention for article published in BMC Medical Genomics, July 2018

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment. https://t.co/rzElVqzof1

Novel digenic inheritance of PCDH15 https://t.co/TmbN3Fnkol and USH1G https://t.co/FT3cbj92ti variants underlies profound non-syndromic #HearingLoss in #consanguineous family from #Pakistan https://t.co/kQMgAy6Kv1

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