WNT11, a new gene associated with early onset osteoporosis, is required for osteoblastogenesis

Monogenic early onset osteoporosis (EOOP) is a rare disease defined by low bone mineral density (BMD) that results in increased risk of fracture in children and young adults. Although several causative genes have been identified, some of the EOOP causation remains unresolved. Whole-exome sequencing...

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Detalles Bibliográficos
Autores principales: Caetano da Silva, Caroline, Edouard, Thomas, Fradin, Melanie, Aubert-Mucca, Marion, Ricquebourg, Manon, Raman, Ratish, Salles, Jean Pierre, Charon, Valérie, Guggenbuhl, Pascal, Muller, Marc, Cohen-Solal, Martine, Collet, Corinne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122655/
https://www.ncbi.nlm.nih.gov/pubmed/34875064
http://dx.doi.org/10.1093/hmg/ddab349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122655/
https://www.ncbi.nlm.nih.gov/pubmed/34875064
http://dx.doi.org/10.1093/hmg/ddab349

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