Association of HLA alleles and haplotypes withCYP21A2gene p. V282L mutation in the Croatian population-Reference-Cited by-同舟云学术

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Association of HLA alleles and haplotypes withCYP21A2gene p. V282L mutation in the Croatian population

Published:2016-10-05 Issue:5 Volume:88 Page:239-244
ISSN:2059-2302
Container-title:HLA
language:en
Short-container-title:HLA

Author:

Grubic Z.¹,Maskalan M.¹,Stingl Jankovic K.¹,Zvecic S.¹,Dumic Kubat K.²,Krnic N.²,Zunec R.¹,Ille J.²,Kusec V.³,Dumic M.⁴

Affiliation:

1. Tissue Typing Centre, Department of Transfusion Medicine and Transplantation Biology; Clinical Hospital Centre Zagreb; Zagreb Croatia

2. Department of Pediatrics; Clinical Hospital Centre Zagreb; Zagreb Croatia

3. Department of Laboratory Diagnosis; Clinical Hospital Centre Zagreb; Zagreb Croatia

4. Department of Pediatrics; School of Medicine; Zagreb Croatia

Publisher

Wiley

Subject

Genetics,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/tan.12907/fullpdf

Reference27 articles.

1. Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency);Dupont;Lancet,1977

2. The structural basis of the multiple forms of human complement component C4;Belt;Cell,1984

3. Structure of the human steroid 21-hydroxylase genes;White;Proc Natl Acad Sci USA,1986

4. Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene;Higashi;Proc Natl Acad Sci USA,1986

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Associations between HLA class II alleles and IgE sensitization to allergens in the Qatar Biobank cohort;Journal of Allergy and Clinical Immunology: Global;2023-08

2. Congenital Adrenal Hyperplasia and Human Leukocyte Antigen B: A Meta-Analysis;Cureus;2023-03-08

3. Detection of novel and confirmation of very rare and rare HLA alleles by next generation sequencing in Croatia;HLA;2020-05-08

4. Revisiting the association of HLA alleles and haplotypes with CYP21A2 mutations in a large cohort of patients with congenital adrenal hyperplasia;Gene;2019-03

5. Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker;Australasian Journal of Dermatology;2019-01-17

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