Journal article

A 5 ' intronic splice site polymorphism leads to a nulll allele of the P2X(7) gene in 1-2% of the Caucasian population

KK Skarratt, SJ Fuller, R Sluyter, LP Dao-Ung, BJ Gu, JS Wiley

FEBS Letters | WILEY | Published : 2005

DOI: 10.1016/j.febslet.2005.03.091

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44Web of Science
50Scopus

Keywords

Polymorphism, Genetic
P2x(7) Receptor
Chronic Lymphocytic-Leukemia
Agonists
Human Monocytes
Point Mutation
Cell Biology
Introns
Reverse Transcriptase Polymerase Chain Reaction
Phagosome-Lysosome Fusion
Female
European Continental Ancestry Group
Rna Splice Sites
Dna Mutational Analysis
Release
Heterozygote
Biophysics
India
Alleles
Mutation
Adult
Aged
Humans
Ala Polymorphism
Male
Virulent Mycobacterium-Tuberculosis
5 ' Splice Site
Biochemistry & Molecular Biology
Gene Frequency
Science & Technology
Polymorphism
Middle Aged
Life Sciences & Biomedicine
Human Macrophages
Receptors, Purinergic P2
Receptors, Purinergic P2x7
Phospholipase-D Activation
Receptor