Novel exostosin-2 mutation identified in a Chinese family with hereditary multiple osteochondroma

Hereditary multiple osteochondroma (HMO) is an autosomal dominant genetic disorder characterized by multiple outgrowing bony tumors capped by cartilage, generally affecting the metaphyses. The disease is known as hereditary multiple exostoses, familial exostosis, multiple cartilaginous exostoses or...

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Detalles Bibliográficos
Autores principales: Ruan, Weiwei, Cao, Li, Chen, Zhonghua, Kong, Mingxiang, Bi, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835906/
https://www.ncbi.nlm.nih.gov/pubmed/29541207
http://dx.doi.org/10.3892/ol.2018.7838

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835906/
https://www.ncbi.nlm.nih.gov/pubmed/29541207
http://dx.doi.org/10.3892/ol.2018.7838

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