Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1999.tb01096.x/fullpdf
Reference43 articles.
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2. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Pediatrics,1988
3. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man;White;Proc Natl Acad Sci USA,1985
4. Mapping the steroid 21- hydroxylase adjacent complement component C4 genes in HLA major histocompatibility complex in man;Carroll;Proc Natl Acad Sci USA,1985
5. Structure of human steroid 21- hydroxylase genes;White;Proc Natl Acad Sci USA,1986
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1. Mutation distributions among patients with congenital adrenal hyperplasia from five regions of Brazil: a systematic review;Archives of Endocrinology and Metabolism;2023-02-03
2. Higher Body Fat but Similar Phase Angle Values in Patients with the Classical Form of Congenital Adrenal Hyperplasia in Comparison to a Control Group;Nutrients;2022-12-06
3. Normal ambulatory blood pressure in young adults with 21-hydroxylase enzyme deficiency undergoing glucocorticoid replacement therapy;Archives of Endocrinology and Metabolism;2022
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5. Cardiovascular dysfunction risk in young adults with congenital adrenal hyperplasia caused by 21‐hydroxylase enzyme deficiency;International Journal of Clinical Practice;2021-05
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