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...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. ...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 ...