Article
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3.
Human molecular genetics - 1 Aug 1995
Bitner-Glindzicz M, Turnpenny P, Höglund P, Kääriäinen H, Sankila E M, van der Maarel S M, de Kok Y J, Ropers H H, Cremers F P, Pembrey M
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