HESX1 Polyclonal Antibody, 100ul Monoclonal Antibodies Mutations in this gene cause

Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3

neuronal growth cone collapse and cell migration

KAT7 is a gene on chromosome 17q21

This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region

likely induces apoptosis in tumor and immature cells

HESX1 Polyclonal Antibody, 100ul Monoclonal Antibodies Mutations in this gene causeThis gene encodes a conserved homeobox protein that is a transcriptional repressor in the developing forebrain and pituitary gland. Mutations in this gene are associated with septooptic dysplasia, HESX1 related growth hormone deficiency, and combined pituitary hormone deficiency.