Work

Biochemical and genetic diagnosis of 21-hydroxylase deficiency

Year: 2015

Type: review

Source: Endocrine

DOI: 10.1007/s12020-015-0731-6

Authors: Henrik Falhammar, Anna Wedell, Anna Nordenström

Institutions: Karolinska University Hospital, Karolinska Institutet

Language: English

Topic: Sexual Differentiation and Disorders

Subfield: Endocrinology, Diabetes and Metabolism

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Magnus Bergvalls Stiftelse

OpenAlex ID: W1224223593

FWCI: 1.142

Cites: 94

Cited by: 84

Related to: 10