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Novel compound heterozygous synonymous and missense variants in the ...
Autosomal dominant non-syndromic hearing loss caused by a novel ...
Distinct effects of two hearing loss–associated mutations in the ...
Modifier controls severity of a novel dominant low-frequency MyosinVIIA ...
Novel compound heterozygous MYO7A mutations in Moroccan families with ...
Symptoms and Testing information for MYO7A Gene Deafness Autosomal Dominant
Identification of a novel compound heterozygous pathogenic variant in ...
Systematic genetic assessment of hearing loss using whole-genome ...
Clinical Heterogeneity Associated with MYO7A Variants Relies on ...
Frontiers | Pathophysiology of human hearing loss associated with ...
A Novel Mutation Located in the N‐Terminal Domain of MYO15A Caused ...
Sensorineural Hearing Loss in Patients With the m.1555A>G Mutation in ...
Hearing in 44–45 year olds with m.1555A>G, a genetic mutation ...
Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing ...
Phenotypic observations of Myo7a mutant strains. (A) Hearing profile of ...
一个非综合征性遗传性耳聋家系中 MYO7A 基因的突变分析
Structural mapping of deafness causing myosin-15 mutations. (A) Ribbon ...
一个常染色体隐性遗传性耳聋家系中 MYO7A 基因的突变与遗传分析
(PDF) Autosomal dominant non-syndromic hearing loss caused by a novel ...
Novel missense mutations in MYO7A underlying postlingual high- or low ...
The Role of Primary Mitochondrial Disorders in Hearing Impairment: An ...
Insights into the Biology of Hearing and Deafness Revealed by Single ...
MYO7A基因突变与遗传性耳聋_word文档在线阅读与下载_无忧文档
MYO7A is required for the functional integrity of the mechanoelectrical ...
Myosin genes and mutations in the Middle Eastern population | Download ...
(PDF) Identification and Functional Study of a New Missense Mutation in ...
Three different mutations of myosin IIIA are associated with deafness ...
The clinical and genetic spectrum of twenty-six individuals with ...
(PDF) Investigation of MYO15A and MYO7A Mutations in Iranian Patients ...
Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in ...
Aminoglycoside-associated nonsyndromic deafness and speech disorder in ...
The effect of novel mutations on the structure and enzymatic activity ...
Expansion of phenotypic spectrum of MYO15A pathogenic variants to ...
Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic ...
Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and ...
Figure 1 from The Promise of Whole-Exome Sequencing in Detecting Novel ...
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive ...
Identification of novel compound heterozygous mutations of the MYO15A ...
Phenotypic expression of maternally inherited deafness is affected by ...
Figure 1 from Three MYO15A Mutations Identified in One Chinese Family ...
(PDF) Novel Compound Heterozygous MYO15A Splicing Variants in Autosomal ...
(PDF) Post-lingual non-syndromic hearing loss phenotype: a polygenic ...
Figure 1 from Compound Heterozygous Mutations in TMC1 and MYO15A Are ...
A: The patient has compound heterozygous MYO15A mutations (c.[9478C>T ...
Three MYO15A Mutations Identified in One Chinese Family with Autosomal ...
Genotype-phenotype correlation analysis of MYO15A variants in autosomal ...
MYO15A 基因罕见突变导致常染色体隐性遗传性耳聋的遗传学及听力表型分析
Figure 1 from Prioritized sequencing of the second exon of MYO15A ...
Prioritized sequencing of the second exon of MYO15A reveals a new ...
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 ...
The number of previously reported MYO15A variants with a milder ...
Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi ...
Report of a Novel Splicing Mutation in the MYO15A Gene in a Patient ...
(PDF) Identification of a Novel MYO15A Mutation in a Chinese Family ...
Hearing loss as an autosomal recessive phenotype associated with ...
(PDF) Novel myosin mutations for hereditary hearing loss revealed by ...
#stereocilia #myo15a #actin #hearingloss #audiology #research… | Eighth ...
(PDF) Mutation Detection in MYO15A Gene in an Iranian Family with Non ...
The spectrum of MYO15A variants in different populations. The black ...
Pedigrees of families with CDH23, MYO15A, TECTA, and WFS1 mutations ...
Characterising the spectrum of autosomal recessive hereditary hearing ...
Knock-In Mice with Myo3a Y137C Mutation Displayed Progressive Hearing ...
(PDF) Loss-of-function mutations in MYO15A and OTOF cause non-syndromic ...
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish ...
Mutations associated with hearing loss that affect specific splice ...
The Prevalence and Clinical Characteristics of MYO3A-Associated Hearing ...
Identification of Novel Compound Heterozygous MYO15A Mutations in Two ...
Identification of a novel MYO6 mutation associated with autosomal ...
Targeted Next‐Generation Sequencing Identified Compound Heterozygous ...
Hearing Features and Cochlear Implantation Outcomes in Patients With ...
Genetic Underpinnings and Audiological Characteristics in Children With ...
