COLEC10 is mutated in 3MC patients and regulates early craniofacial development

3MC syndrome is an autosomal recessive heterogeneous disorder with features linked to developmental abnormalities. The main features include facial dysmorphism, craniosynostosis and cleft lip/palate; skeletal structures derived from cranial neural crest cells (cNCC). We previously reported that lect...

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Detalles Bibliográficos
Autores principales: Munye, Mustafa M., Diaz-Font, Anna, Ocaka, Louise, Henriksen, Maiken L., Lees, Melissa, Brady, Angela, Jenkins, Dagan, Morton, Jenny, Hansen, Soren W., Bacchelli, Chiara, Beales, Philip L., Hernandez-Hernandez, Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373641/
https://www.ncbi.nlm.nih.gov/pubmed/28301481
http://dx.doi.org/10.1371/journal.pgen.1006679

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373641/
https://www.ncbi.nlm.nih.gov/pubmed/28301481
http://dx.doi.org/10.1371/journal.pgen.1006679

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