Genotype-Phenotype Correlation for DFNA22: Characterization of Non-Syndromic, Autosomal Dominant, Progressive Sensorineural Hearing Loss due to MYO6 Mutations
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A. Zarowski | V. Topsakal | J. van Dinther | G. Van Camp | E. Offeciers | N. Hilgert | L. Tranebjærg | N. D. Rendtorff | P. H. Van de Heyning