Lv1
50 积分 2025-01-27 加入
Targeted and Genomewide NGS Data Disqualify Mutations inMYO1A, the “DFNA48Gene”, as a Cause of Deafness
8小时前
已关闭
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness‐41) and P2RX2 Gene Mutations: A Phenotype–Genotype Study
9小时前
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Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
9小时前
已完结
High Prevalence of MYO6 Variants in an Austrian Patient Cohort With Autosomal Dominant Hereditary Hearing Loss
1天前
已完结
Characterization of Sensorineural Hearing Loss in Patients With MYH9-Related Disease: A Systematic Review
3天前
已完结
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