PMR1 Monoclonal Antibody, 100ul Monoclonal Antibody Preparation Mutations in this gene are
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PMR1 Monoclonal Antibody, 100ul Monoclonal Antibody Preparation Mutations in this gene areThe protein encoded by this gene belongs to the family of P type cation transport ATPases. This magnesium dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
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