Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)
DIAPH1 相关常染色体显性听力损失 (DFNA1) 的临床和分子表型的扩展
期刊:Clinical Genetics
影响因子:2.9
doi:10.1111/cge.12915
C Neuhaus, R Lang-Roth, U Zimmermann, R Heller, T Eisenberger, M Weikert, S Markus, M Knipper, H J Bolz
