SVIL Polyclonal Antibody, 20ul Isothermal Amplification Mutations in this gene cause

Mutations in this gene cause Charcot-Marie-Tooth disease| type 2A1

imprinting

The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions

This enzyme catalyzes the stepwise oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX| a precursor of heme

which are asymmetrically expressed in the developing ventricular chambers and play an essential role in cardiac morphogenesis

SVIL Polyclonal Antibody, 20ul Isothermal Amplification Mutations in this gene causeThis gene encodes a bipartite protein with distinct amino and carboxy terminal domains. The amino terminus contains nuclear localization signals and the carboxy terminus contains numerous consecutive sequences with extensive similarity to proteins in the gelsolin family of actin binding proteins, which cap, nucleate, and or sever actin filaments. The gene product is tightly associated with both actin filaments and plasma membranes, suggesting a role