21-Hydroxylase deficiency in Brazil-Reference-Cited by-同舟云学术

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21-Hydroxylase deficiency in Brazil

Published:2000-10 Issue:10 Volume:33 Page:1211-1216
ISSN:0100-879X
Container-title:Brazilian Journal of Medical and Biological Research
language:
Short-container-title:Braz J Med Biol Res

Author:

Bachega T.A.S.S.¹,Billerbeck A.E.C.¹,Madureira G.¹,Marcondes J.A.M.¹,Longui C.A.²,Leite M.V.³,Arnhold I.J.P.¹,Mendonça B.B.¹

Affiliation:

1. Universidade de São Paulo, Brasil

2. Santa Casa, Brasil

3. Universidade Federal do Rio Grande do Norte, Brasil

Publisher

FapUNIFESP (SciELO)

Subject

Cell Biology,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Immunology,Physiology,Biochemistry,General Neuroscience,Biophysics

Link

http://www.scielo.br/pdf/bjmbr/v33n10/3765m.pdf

Reference28 articles.

1. The Metabolic Basis of Inherited Disease;New MI,1989

2. Advance of Human Genetics;Morel Y,1991

3. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man;Carroll MC;Proceedings of the National Academy of Sciences, USA,1985

4. Structure of human steroid 21-hydroxylase genes;White PC;Proceedings of the National Academy of Sciences, USA,1986

5. Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene;Higashi Y;Proceedings of the National Academy of Sciences, 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. 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. Characterization of the CYP21A2 Gene Mutations in Children with Classic Congenital Adrenal Hyperplasia;Indian Journal of Pediatrics;2022-01-30

3. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Gene;2013-09

4. Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan;Russian Journal of Genetics;2008-10

5. Estudo multicêntrico de pacientes brasileiros com deficiência da 21-hidroxilase: correlação do genótipo com o fenótipo;Arquivos Brasileiros de Endocrinologia & Metabologia;2004-10

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