E380D: A novel point mutation of CYP21 in an HLA‐homozygous patient with salt‐losing congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

Subjects

Subjects :

Genetics
Genetics (clinical)

Details

ISSN :

10981004 and 10597794

Volume :

9

Database :

OpenAIRE

Journal :

Human Mutation

Accession number :

edsair.doi...........8eef2e49ca4a9a1c812d2e8666e46e35

Full Text :

https://doi.org/10.1002/(sici)1098-1004(1997)9:2<181::aid-humu12>3.3.co;2-c