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MYO7A in Biological Products

Mouse Anti-Human MYO7A Monoclonal Antibody, Unconjugated, Clone 1D3 from Abnova Corporation

Description: Mouse monoclonal antibody raised against a partial recombinant MYO7A. NCBI Entrez Gene ID = MYO7A...
Company:Abnova Corporation
MYO7A in other areas

MYO7A - Wikipedia, the free encyclopedia

Myosin VIIA (MYO7A) is a member of the unconventional myosin superfamily of proteins. Myosins are actin binding molecular motors that use the enzymatic conversion of ATP - ADP + inorganic phosphate (Pi) to provide the energy for movement.

MYO7A - myosin VIIA - Genetics Home Reference

nonsyndromic deafness - caused by mutations in the MYO7A gene ... A few studies have associated MYO7A mutations with an autosomal recessive form ...

MYO7A Gene Test for Usher Syndrome Type I

Footer ... Mutations in the MYO7A gene account for approximately 60% of Type 1 ... MYO7A mutations have also been reported in several families with recessive ...

MYO7A Gene Test for Usher Syndrome Type I

Pathogenic mutations in MYO7A gene are found in about 60% of patients with Usher ... but the majority is clustered in the exons encoding the MYO7A motor domain. ...

276903

Database of Single Nucleotide Polymorphism ... SNP linked to Gene MYO7A(geneID:4647) Via Contig Annotation. rs# on all gene models to Batch Query ...

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in ...

Severe Myo7a mutations result in a disorganization of the ... Myo7a mutations do not cause visible changes in hair cell ... for Myo15 and Myo6, Myo7a or pi ...
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