Osteopetrosis and Its Relevance for the Discovery of New Functions Associated with the Skeleton

Osteopetrosis is a rare genetic disorder characterized by an increase of bone mass due to defective osteoclast function. Patients typically displayed spontaneous fractures, anemia, and in the most severe forms hepatosplenomegaly and compression of cranial facial nerves leading to deafness and blindn...

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Detalles Bibliográficos
Autores principales: Coudert, Amélie E., de Vernejoul, Marie-Christine, Muraca, Maurizio, Del Fattore, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385565/
https://www.ncbi.nlm.nih.gov/pubmed/25873953
http://dx.doi.org/10.1155/2015/372156

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385565/
https://www.ncbi.nlm.nih.gov/pubmed/25873953
http://dx.doi.org/10.1155/2015/372156

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