Work

Point mutations in Italian patients with classic, non-classic, and cryptic forms of steroid 21-hydroxylase deficiency

Year: 1996

Type: article

Study design: Observational Study

Source: Human Genetics

DOI: 10.1007/s004390050280

Authors: P. Carrera, Laura Bordone, Tiziana Azzani, Valeria Brunelli, Maria Paola Garancini, Giuseppe Chiumello, Maurizio Ferrari

Institutions: IRCCS Ospedale San Raffaele, University of Milan

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: W2006550622

FWCI: 2.663

Cites: 13

Cited by: 71

Related to: 10