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A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel’s syndrome
E. A. de Zwart-Storm, M. van Geel, E. Veysey, S. Cooper, P. M. Steijlen, Patricia E.M. Martin, M. A.M. van Steensel
Research output: Contribution to journal › Article › peer-review
21
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(Scopus)