Work

The frequency of eight common point mutations in CYP21 gene in Iranian patients with congenital adrenal hyperplasia.

Year: 2008

Type: article

Study design: Observational Study

Source: PubMed

Authors: Ali Ramazani, Kimia Kahrizi, Maryam Razaghiazar, Nejat Mahdieh, Paul Koppens

Institutions: Zanjan University of Medical Sciences, University of Social Welfare and Rehabilitation Sciences, Iran University of Medical Sciences, Rasool Akram Hospital, Tarbiat Modares University, Erasmus MC, Erasmus MC - Sophia Children’s Hospital

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

OpenAlex ID: W2136269669

FWCI: 1.371

Cites: 23

Cited by: 31

Related to: 10