"A novel mutation of X‐linked recessive deafness gene POU3F4 in a boy with congenital deafness"

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To report an interstitial deletion of Xq21.1 in chromosome X in a boy with congenital deafness. Click to show full abstract

To report an interstitial deletion of Xq21.1 in chromosome X in a boy with congenital deafness.

Keywords: mutation linked; novel mutation; congenital deafness; linked recessive; boy congenital; deafness

Journal Title: Laryngoscope Investigative Otolaryngology
Year Published: 2022

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