First insights into the genetics of 21‐hydroxylase deficiency in the Roma population-Reference-Cited by-同舟云学术

First insights into the genetics of 21‐hydroxylase deficiency in the Roma population

Published:2021-03-02 Issue:1 Volume:95 Page:41-46
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Kocova Mirjana¹^ORCID,Anastasovska Violeta²,Petlichkovski Aleksandar³^ORCID,Falhammar Henrik⁴⁵^ORCID

Affiliation:

1. Department of Endocrinology and Genetics University Pediatric Hospital, Skopje University “Ss Cyril and Methodius” Skopje Republic of North Macedonia

2. Genetic Laboratory University Pediatric Hospital, Skopje University “Ss Cyril and Methodius” Skopje Republic of North Macedonia

3. Institute of Immunology and Human genetics Medical Faculty University “Ss Cyril and Methodius” Skopje Republic of North Macedonia

4. Department of Endocrinology, Metabolism and Diabetes Karolinska University Hospital Stockholm Sweden

5. Departement of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14447

Reference41 articles.

1. Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

2. CYP21A2mutation update: Comprehensive analysis of databases and published genetic variants

3. Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

4. Congenital adrenal hyperplasia

5. Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene

Cited by 4 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. The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population;Frontiers in Endocrinology;2023-05-31

2. Genetic Determinants of Leisure-Time Physical Activity in the Hungarian General and Roma Populations;International Journal of Molecular Sciences;2023-02-26

3. Genotype‐phenotype association in congenital adrenal hyperplasia due to 21‐hydroxylase deficiency in children;Clinical Endocrinology;2022-12-15

4. Characteristics of In2G Variant in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency;Frontiers in Endocrinology;2022-01-24