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Frontiers Pathophysiology of human hearing loss associated with

Spectrum of MYO7A Mutations in an Indigenous South African Population

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Frontiers Pathophysiology of human hearing loss associated with

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Myosin 7a is required for maintaining the transducing stereocilia and

MYO7A Deafness DNA Test ZAR 6700 Early Detection for South Africans

Distinct effects of two hearing lossassociated mutations in the

Spectrum of MYO7A Mutations in an Indigenous South African Population

Frontiers Pathophysiology of human hearing loss associated with

Distinct effects of two hearing lossassociated mutations in the

The effect of novel mutations on the structure and enzymatic activity

Novel myosin mutations for hereditary hearing loss revealed by targeted

Distinct effects of two hearing lossassociated mutations in the

Frontiers Pathophysiology of human hearing loss associated with

Novel myosin mutations for hereditary hearing loss revealed by targeted

Frontiers Pathophysiology of human hearing loss associated with

Myosin 7a is required for maintaining the transducing stereocilia and

Frontiers Pathophysiology of human hearing loss associated with

Structural mapping of deafness causing myosin15 mutations A Ribbon

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing

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PDF Nonmuscle myosin heavy chain IIA mutation and hearing loss in two

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Myosin genes and mutations in the Middle Eastern population Download

Nonmuscle Myosin HeavyChain Gene MYH14 Is Expressed in Cochlea and

A Domain organization of myosinVIIA and gene structure of MYO7A The

Schema of myosin VIIa domains with mutations identified in MYO7A The

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Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in

Myosin genes and mutations in the Middle Eastern population Download

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Identification and Functional Study of a New Missense Mutation in the

Frontiers Pathophysiology of human hearing loss associated with

Nonmuscle Myosin HeavyChain Gene MYH14 Is Expressed in Cochlea and

Mutations of MYO6 Are Associated with Recessive Deafness DFNB37 The

Structural mapping of deafness causing myosin15 mutations A Ribbon

Novel compound heterozygous synonymous and missense variants in the

Schematic diagram of Myo7a protein structure showing the location of

Structural mapping of deafness causing myosin15 mutations A Ribbon

Overview of known MYO15A variants and related hearing phenotypes The

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Clinical Heterogeneity Associated with MYO7A Variants Relies on

A Myo6 Mutation Destroys Coordination between the Myosin Heads

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Clinical Heterogeneity Associated with MYO7A Variants Relies on

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Novel compound heterozygous synonymous and missense variants in the

The clinical and genetic spectrum of twentysix individuals with

A novel missense variant in MYO3A is associated with autosomal dominant

Genetic causes of moderate to severe hearing loss point to modifiers PMC

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The spectrum of MYO15A variants in different populations The black

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The number of previously reported MYO15A variants with a milder

Overview of known MYO15A variants and related hearing phenotypes The

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Frontiers A Novel Mouse Model of MYO7A USH1B Reveals Auditory and

Novel compound heterozygous MYO7A mutations in Moroccan families with

A novel compound heterozygous mutation in the MYO15A gene in autosomal

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Novel compound heterozygous MYO7A mutations in Moroccan families with

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A missense mutation in MYO7A is associated with bilateral deafness and

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Figure 1 from Rare coding variants involving MYO7A and other genes

The Prevalence and Clinical Characteristics of MYO3AAssociated Hearing

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Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing

Schematic diagram of Myo7a protein structure showing the location of

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A DNA Variant within the MYO7A Promoter Regulates YY1 Transcription

A novel compound heterozygous mutation in the MYO15A gene in autosomal

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Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing

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MYO7A is required for the functional integrity of the mechanoelectrical

Identification of a Novel MYO15A Mutation in a Chinese Family with

Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3

MYO7A is required for the functional integrity of the mechanoelectrical

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The Prevalence and Clinical Characteristics of MYO3AAssociated Hearing

Identification of novel compound heterozygous mutations of the MYO15A

A Novel Mutation Located in the NTerminal Domain of MYO15A Caused

SEM analysis of cochlear hair cells in Myo7a mutants and Myo15 Myo7a

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish

The number of previously reported MYO15A variants with a milder

Mutations in MYO6 causing dominant and recessive hearing loss with the

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A missense mutation in MYO7A is associated with bilateral deafness and

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PDF Novel mutations of MYO15A associated with profound deafness in

Multiple Mutations ofMYO1A a CochlearExpressed Gene in Sensorineural

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Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3

Figure 1 from Compound Heterozygous Mutations in TMC1 and MYO15A Are

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