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50 积分 2025-01-27 加入
Preliminary evidence for enhanced auditory cortex activation and mental development after gene therapy in children with autosomal recessive deafness 9
10小时前
已完结
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness‐41) and P2RX2 Gene Mutations: A Phenotype–Genotype Study
3个月前
已关闭
Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation
3个月前
已完结
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss
3个月前
已完结
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss
3个月前
已完结
Whole exome sequencing identifies SCD5 as a novel causative gene for autosomal dominant nonsyndromic deafness
3个月前
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Mutations in PLS1 , encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss
3个月前
已完结
Targeted and Genomewide NGS Data Disqualify Mutations inMYO1A, the “DFNA48Gene”, as a Cause of Deafness
3个月前
已关闭
Progressive Dominant Hearing Loss (Autosomal Dominant Deafness‐41) and P2RX2 Gene Mutations: A Phenotype–Genotype Study
3个月前
已关闭
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
3个月前
已完结
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