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The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy

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Year: 2012
Type: article
Study design: Observational Study
Source: Journal of Medical Genetics
DOI: 10.1136/jmedgenet-2012-101251
Authors: Jean-Benoît Courcet, Laurence Faivre, Perrine Malzac, Alice Masurel-Paulet, Estelle Lopez, Patrick Callier, Laetitia Lambert, Martine Lemesle, Julien Thevenon, Nadège Gigot, Laurence Duplomb, Clémence Ragon, Nathalie Marle, Anne-Laure Mosca-Boidron, Frédéric Huet, Christophe Philippe, Anne Moncla, Christel Thauvin-Robinet
Institutions: Université de Bourgogne, CHU Dijon Bourgogne, Hôpital de la Timone, Centre Hospitalier Régional et Universitaire de Nancy
Language: English

Topic: Genetics and Neurodevelopmental Disorders
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Conseil régional de Bourgogne-Franche-Comté
OpenAlex ID: W2143060505
FWCI: 3.375
Cites: 32
Cited by: 127
Related to: 10
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