Work

[Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to 21-hydroxylase enzyme deficiency].

Year: 2001

Type: article

Study design: Observational Study

Source: PubMed

Authors: A Dardis, R Marino, I Bergadá, M E Escobar, M Gryngarten, M A Rivarola, A Belgorosky

Institution: Garrahan Hospital

Language: Spanish

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

OpenAlex ID: W2400772636

FWCI:

Cites:

Cited by: 1

Related to: 10