Osteoclastogenesis inhibition by mutated IGSF23 results in human osteopetrosis

OBJECTIVES: Osteopetrosis is a rare inherited skeletal disease characterized by increased bone mineral density due to the loss of osteoclast function or differentiation potential. MATERIALS AND METHODS: The study involved a Chinese patient with osteopetrosis (the proband) and her immediate family me...

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Detalles Bibliográficos
Autores principales: Yuan, Ying, Yang, Li, Liu, Ting, Zhang, Hong, Lu, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6869366/
https://www.ncbi.nlm.nih.gov/pubmed/31560140
http://dx.doi.org/10.1111/cpr.12693

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6869366/
https://www.ncbi.nlm.nih.gov/pubmed/31560140
http://dx.doi.org/10.1111/cpr.12693

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