RSK2 Is a Modulator of Craniofacial Development

BACKGROUND: The RSK2 gene is responsible for Coffin-Lowry syndrome, an X-linked dominant genetic disorder causing mental retardation, skeletal growth delays, with craniofacial and digital abnormalities typically associated with this syndrome. Craniofacial and dental anomalies encountered in this rar...

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Detalhes bibliográficos
Main Authors: Laugel-Haushalter, Virginie, Paschaki, Marie, Marangoni, Pauline, Pilgram, Coralie, Langer, Arnaud, Kuntz, Thibaut, Demassue, Julie, Morkmued, Supawich, Choquet, Philippe, Constantinesco, André, Bornert, Fabien, Schmittbuhl, Matthieu, Pannetier, Solange, Viriot, Laurent, Hanauer, André, Dollé, Pascal, Bloch-Zupan, Agnès
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2014
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3885557/
https://ncbi.nlm.nih.gov/pubmed/24416220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0084343
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