All individuals with variants in gene EHHADH

3 entries on 1 page. Showing entries 1 - 3.
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00016189 - PubMed: Zhang 2014 4-generation family, 11 affected (5F, 6M) F;M no China Chinese - - - - DFNA1 nonsyndromic, bilateral, slowly progressive hearing impairment, starting mildly in high frequencies; age onset late 20s, hearing impairment gradually progressed to all frequencies later, eventually reached severe-to-profound in seventh decade; absent or abnormal otoacoustic emission, no evidence of vestibular dysfunction, no inner ear malformation observed by CT scanning 1 11 Tao Yang
00293293 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00395063 K53 PubMed: Zacchia 2021 - F - (Italy) - - - - - retinal disease - 1 1 LOVD
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