Gene Conversion-like Missense Mutations in the Human Cationic Trypsinogen Gene and Insights into the Molecular Evolution of the Human Trypsinogen Family
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference44 articles.
1. Human Molecular Genetics;Strachan,1999
2. Mutation in the CYP21B gene (Ile-172- - - -Asn) causes steroid 21-hydroxylase deficiency;Amor;Proc Natl Acad Sci USA,1988
3. Nonsense mutation causing steroid 21-hydroxylase deficiency;Globerman;J Clin Invest,1988
4. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency;White;Proc Natl Acad Sci USA,1988
5. A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome;Collier;Nature Genet,1993
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