Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

BACKGROUND: Hereditary multiple osteochondromas (HMO), previously named hereditary multiple exostoses (HME), is an autosomal dominant skeletal disorder characterized by the growth of multiple osteochondromas and is associated with bony deformity, skeletal growth reduction, nerve compression, restric...

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Detalles Bibliográficos
Autores principales: Akbaroghli, Susan, Balali, Maryam, Kamalidehghan, Behnam, Saber, Siamak, Aryani, Omid, Meng, Goh Yong, Houshmand, Massoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189706/
https://www.ncbi.nlm.nih.gov/pubmed/28053536
http://dx.doi.org/10.2147/TCRM.S111717

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189706/
https://www.ncbi.nlm.nih.gov/pubmed/28053536
http://dx.doi.org/10.2147/TCRM.S111717

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