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Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss
Pollak A,
Lechowicz U,
Kędra A,
Stawiński P,
Rydzanicz M,
et al.
(2016)
Novel and De Novo Mutations Extend Association of POU3F4 with Distinct Clinical and Radiological Phenotype of Hearing Loss.
PLOS ONE 11(12): e0166618.
https://doi.org/10.1371/journal.pone.0166618