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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Detalhes bibliográficos
Publicado no:Ther Clin Risk Manag
Main Authors: Akbaroghli, Susan, Balali, Maryam, Kamalidehghan, Behnam, Saber, Siamak, Aryani, Omid, Meng, Goh Yong, Houshmand, Massoud
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2016
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5189706/
https://ncbi.nlm.nih.gov/pubmed/28053536
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TCRM.S111717
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