HESX1 Polyclonal Antibody, 20ul Cell Separation and Collection which are congenital abnormalities in
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HESX1 Polyclonal Antibody, 20ul Cell Separation and Collection which are congenital abnormalities inThis 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.
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