A Novel Mutation in SNX10 Gene Causes Malignant Infantile Osteopetrosis

BACKGROUND: Osteopetrosis is a group of genetically heterogonous diseases and the main feature of that is increased bone density due to osteoclast’s abnormality. It has three clinical forms based on inheritance pattern, severity and age of onset: the dominant benign form (ADO), the intermediate form...

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Detalles Bibliográficos
Autores principales: Amirfiroozy, Akbar, Hamidieh, Amir A., Golchehre, Zahra, Rezamand, Azim, Yahyaei, Mahin, Beiranvandi, Fatemeh, Amirfiroozy, Soheyla, Keramatipour, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650739/
https://www.ncbi.nlm.nih.gov/pubmed/29090071

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650739/
https://www.ncbi.nlm.nih.gov/pubmed/29090071

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