Molecular characterization of three new mutations causing C5 deficiency in two non-related families
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Immunology
Reference28 articles.
1. Complement system on the attack in autoimmunity;Atkinson;J. Clin. Invest.,2003
2. Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases;Blencowe;Trends Biochem. Sci.,2002
3. Structural aspects of the human C5 gene. Intron/exon organization, 5′ flanking region features, and characterization of two truncated cDNA clones;Carney;J. Biol. Chem.,1991
4. Listening to silence and understanding nonsense: exonic mutations that affect splicing;Cartegni;Nat. Rev. Genet.,2002
5. The PyMOL Molecular Graphics System;DeLano,2002
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