Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.

Haplotypes of the complement 4 (C4) and steroid 21-hydroxylase [21-OHase; steroid hydrogen-donor: oxygen oxidoreductase (21-hydroxylating), EC 1.14.99.10] repeated gene complex were studied in nine families with at least one member affected with a mild form of 21-OHase deficiency. DNA probes from di...

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Vydáno v:	Proc Natl Acad Sci U S A
Hlavní autoři:	Haglund-Stengler, B, Martin Ritzén, E, Gustafsson, J, Luthman, H
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	National Academy of Sciences 1991
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC52506/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1924294/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.88.19.8352
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