Journal article
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.
Abstract
Mutations in the gene for CD40 ligand are responsible for the X-linked form of hyper IgM syndrome. However, no clinical or laboratory findings that reliably distinguish X-linked disease from other forms of hyper IgM syndrome have been reported, nor are there tests available that can be used to confidently provide carrier detection. To identify efficiently mutations in the gene for CD40 ligand, eight pairs of PCR primers that could be used to …
Authors
Lin Q; Rohrer J; Allen RC; Larché M; Greene JM; Shigeoka AO; Gatti RA; Derauf DC; Belmont JW; Conley ME
Journal
Journal of Clinical Investigation, Vol. 97, No. 1, pp. 196–201
Publisher
American Society for Clinical Investigation
Publication Date
January 1, 1996
DOI
10.1172/jci118389
ISSN
0021-9738
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Base SequenceCD40 LigandChildChild, PreschoolDNA Mutational AnalysisDNA PrimersFemaleGenetic Carrier ScreeningGenetic LinkageHumansHypergammaglobulinemiaImmunoglobulin MInfantLymphocyte ActivationMaleMembrane GlycoproteinsMolecular Sequence DataPedigreePolymerase Chain ReactionPolymorphism, Single-Stranded ConformationalSyndromeT-LymphocytesX Chromosome