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Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears

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Year: 2013
Type: article
Source: The American Journal of Human Genetics
DOI: 10.1016/j.ajhg.2013.10.023
Authors: Christopher T. Gordon, Florence Petit, Peter M. Kroisel, Linda Jakobsen, Roseli Maria Zechi-Ceide, Myriam Oufadem, Christine Bole-Feysot, Solenn Pruvost, Cécile Masson, Frédéric Tores, Thierry Hieu, Patrick Nitschké, Pernille Lindholm, Philippe Pellerin, Maria Leine Guion-Almeida, Nancy Mizue Kokitsu-Nakata, Siulan Vendramini-Pittoli, Arnold Munnich, Stanislas Lyonnet, Muriel Holder-Espinasse, Jeanne Amiel
Institutions: Hôpital Necker-Enfants Malades, Inserm, Institut Necker Enfants Malades, Sorbonne Paris Cité, Institut des Maladies Génétiques Imagine, Université Paris Descartes, Centre Hospitalier Universitaire de Lille, Hôpital Jeanne de Flandre, Medical University of Graz, Herlev Hospital, Copenhagen University Hospital, Universidade de São Paulo, Rigshospitalet, Guy's Hospital
Language: English

Topic: Craniofacial Disorders and Treatments
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: bronze

Funder: Agence Nationale de la Recherche
Award: Institut Hospitalo-Universitaire Imagine
OpenAlex ID: W2068561298
FWCI: 6.374
Cites: 42
Cited by: 75
Related to: 10
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