Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, NR0B1

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, NR0B1

Definition : Molecular assay reagents intended to identify mutations in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene, located at chromosome Xp21.3-p21.2, which encodes for the protein DAX1 that is involved in the development and function of several hormone-producing (endocrine) tissues in the body. This genetic mutation causes congenital adrenal hypoplasia, X-linked adrenal hypoplasia congenital, and Swyer syndrome.

Entry Terms : "Dosage Sensitive Sex Reversal Gene Mutation Reagents" , "XY Fetus Male/Female Reversal Gene Mutation Reagents" , "Male/Female Sex Reversal Gene Mutation Reagents" , "Hypoplasia Gene Mutation Reagents" , "Adrenal Hypoplasia Gene Mutation Reagents" , "Congenital Adrenal Hypoplasia Gene Mutation Reagents" , "NR0B1 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, NR0B1"

UMDC code : 24643

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