Work

CDKN1C mutations: two sides of the same coin

Year: 2014

Type: review

Source: Trends in Molecular Medicine

DOI: 10.1016/j.molmed.2014.09.001

Authors: Thomas Eggermann, Gerhard Binder, Frédéric Brioude, Eamonn R. Maher, Pablo Lapunzina, Maria Vittoria Cubellis, Ignacio Bergadá, Dirk Prawitt, Matthias Begemann

Institutions: Universitätsklinikum Aachen, RWTH Aachen University, University Children's Hospital Tübingen, University of Tübingen, Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, University of Cambridge, NIHR Cambridge Biomedical Research Centre, Hospital Universitario La Paz, Instituto de Salud Carlos III, University of Naples Federico II, Consejo Nacional de Investigaciones Científicas y Técnicas, Hospital General de Niños Ricardo Gutierrez, Johannes Gutenberg University Mainz

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Ipsen, Division of Materials Research

OpenAlex ID: W2074322136

FWCI: 1.214

Cites: 66

Cited by: 99

Related to: 10