RGAG1 Polyclonal Antibody, 100ul Thermo Mix Mutations in MYL3 have been

Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy

a serine/threonine protein kinase catlytic domain in the central region

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Chloride intracellular channel 4 (CLIC4) protein

The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope

RGAG1 Polyclonal Antibody, 100ul Thermo Mix Mutations in MYL3 have beenRGAG1 (Retrotransposon Gag Domain Containing 1) is a Protein Coding gene. Diseases associated with RGAG1 include non syndromic x linked intellectual disability.