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4.8.1467
4.8.1467
http://dx.doi.org/10.1093/HMG/4.8.1467
Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3
P356
Q28290728-ABEE741E-396F-4B77-931E-65606A6FD4B3
P356
4.8.1467
http://dx.doi.org/10.1093/HMG/4.8.1467