Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene-Reference-Cited by-同舟云学术

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Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene

Published:2012-12-12 Issue:1 Volume:5 Page:98-112
ISSN:1759-6653
Container-title:Genome Biology and Evolution
language:en
Short-container-title:

Author:

Bánlaki Zsófia,Szabó Julianna Anna,Szilágyi Ágnes,Patócs Attila,Prohászka Zoltán,Füst George,Doleschall Márton

Publisher

Oxford University Press (OUP)

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

Link

http://academic.oup.com/gbe/article-pdf/5/1/98/17917965/evs121.pdf

Reference79 articles.

1. Genome structural variation discovery and genotyping;Alkan;Nat Rev Genet.,2011

2. Median-joining networks for inferring intraspecific phylogenies;Bandelt;Mol Biol Evol.,1999

3. Fine-tuned characterization of RCCX copy number variants and their relationship with extended MHC haplotypes;Banlaki;Genes Immun.,2012

4. ACTH-induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non-functional adrenal incidentaloma;Banlaki;Clin Endocrinol.,2012

5. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in Caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease;Blanchong;J Exp Med.,2000

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1. Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation;PLOS ONE;2022-12-01

2. CAH-X Syndrome: Genetic and Clinical Profile;Molecular Diagnosis & Therapy;2022-04-27

3. Capturing SNP Association across the NK Receptor and HLA Gene Regions in Multiple Sclerosis by Targeted Penalised Regression Models;Genes;2021-12-29

4. Genes and Pseudogenes: Complexity of the RCCX Locus and Disease;Frontiers in Endocrinology;2021-07-30

5. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers–Danlos Syndrome with 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2020-04-15

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