additional file 1 table s1 of a novel pore region mutation c 887gâ âa p g296d in kcnq4 causing hearing loss in a chinese family with autosomal dominant non syndromic deafness 2
DOI:
10.6084/m9.figshare.c.3726256_d1
Publication Date:
2017-01-01
AUTHORS (7)
ABSTRACT
Potential deafness causing variants found by NGS. (DOCX 14 kb)
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