Work

Compound Heterozygous and Homozygous Mutations of the TSHβ Gene as a Cause of Congenital Central Hypothyroidism in Europe

Year: 2004

Type: article

Source: Hormone Research in Paediatrics

DOI: 10.1159/000080071

Authors: Beate Karges, Bruno LeHeup, Eugen Schoenle, Cintia Castro-Correia, Manuel Fontoura, Roland Pfäffle, Werner Andler, Klaus-Michael Debatin, Wolfram Karges

Institutions: Universität Ulm, University of Zurich, University Children's Hospital Zurich, Universidade do Porto, University Hospital Leipzig, Leipzig University, Witten/Herdecke University

Language: English

Topic: Thyroid Disorders and Treatments

Subfield: Endocrinology, Diabetes and Metabolism

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2018908196

FWCI: 0.968

Cites: 25

Cited by: 32

Related to: 10