Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.

Corticosterone methyloxidase II (CMO-II) deficiency is an autosomal recessive disorder of aldosterone biosynthesis, characterized by an elevated ratio of 18-hydroxycorticosterone to aldosterone in serum. It is genetically linked to the CYP11B1 and CYP11B2 genes that, respectively, encode two cytochr...

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發表在:	Proc Natl Acad Sci U S A
Principais autores:	Pascoe, L, Curnow, K M, Slutsker, L, Rösler, A, White, P C
格式:	Artigo
語言:	Inglês
出版:	National Academy of Sciences 1992
主題:	Research Article
在線閱讀:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC49215/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1594605/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.11.4996
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