Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency
Year: 1995
Type: article
Study design: Observational Study
Source: Human Mutation
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2002884605
