Analysis of theCYP21A2Gene with Intergenic Recombination and Multiple Gene Deletions in the RCCX Module
Author:
Affiliation:
1. Graduate Institute of Cell and Molecular Biology, Taipei Medical University, Taipei, Taiwan.
2. School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan.
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical),General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0080
Reference37 articles.
1. Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B
2. Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4
3. Deficiencies of Human Complement Component C4a and C4b and Heterozygosity in Length Variants of RP-C4-CYP21-TNX (Rccx) Modules in Caucasians
4. A new CYP21A1P/CYP21A2chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form
5. Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients
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