A novel mutation of X‐linked recessive deafness gene POU3F4 in a boy with congenital deafness
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DOI: 10.1002/lio2.850
Abstract: To report an interstitial deletion of Xq21.1 in chromosome X in a boy with congenital deafness. read more here.
Keywords: mutation linked; novel mutation; congenital deafness; linked recessive ... See more keywords