Home > Specialties > IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, MECP2

IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, MECP2

Definition : Molecular assay reagents intended to identify mutations in the methyl CpG binding protein 2 (MECP2) gene, located at chromosome Xq28, which encodes for a protein essential for normal brain development. Mutations at this locus have been identified in patients with Rett syndrome, an early-onset, almost exclusively female, disease.

Entry Terms : "X-Linked Mental Retardation Gene Mutation Reagents" , "Neonatal Encephalopathy Gene Mutation Reagents" , "Rett Syndrome Gene Mutation Reagents" , "MECP2 Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, MECP2"

UMDC code : 24602

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1-2 of 2 Match(es).

Mayo Medical Laboratories

Company Type: Parent

University of Pittsburgh Medical Center

Company Type: Parent

1-2 of 2 Match(es).

 

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