Clinical and functional heterogeneity associated with the disruption of retinoic acid receptor beta
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Published:2023-08
Issue:8
Volume:25
Page:100856
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Caron Véronique, Chassaing Nicolas, Ragge Nicola, Boschann Felix, Ngu Angelina My-Hoa, Meloche Elisabeth, Chorfi Sarah, Lakhani Saquib A., Ji Weizhen, Steiner Laurie, Marcadier Julien, Jansen Philip R., van de Pol Laura A., van Hagen Johanna M., Russi Alvaro Serrano, Le Guyader Gwenaël, Nordenskjöld Magnus, Nordgren Ann, Anderlid Britt-Marie, Plaisancié Julie, Stoltenburg Corinna, Horn Denise, Drenckhahn Anne, Hamdan Fadi F., Lefebvre Mathilde, Attie-Bitach Tania, Forey Peggy, Smirnov Vasily, Ernould Françoise, Jacquemont Marie-Line, Grotto Sarah, Alcantud Alberto, Coret Alicia, Ferrer-Avargues Rosario, Srivastava Siddharth, Vincent-Delorme Catherine, Romoser Shelby, Safina Nicole, Saade Dimah, Lupski James R., Calame Daniel G., Geneviève David, Chatron Nicolas, Schluth-Bolard Caroline, Myers Kenneth A., Dobyns William B., Calvas Patrick, Salmon Caroline, Holt Richard, Elmslie Frances, Allaire Marc, Prigozhin Daniil M., Tremblay André, Michaud Jacques L.ORCID
Funder
Muscular Dystrophy Association Wellcome Trust Spastic Paraplegia Foundation Canadian Institutes of Health Research Agence nationale de la recherche National Institutes of Health
Subject
Genetics (clinical)
Cited by
4 articles.
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