A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDG

Multiple osteochondromatosis (MO), or EXT1/EXT2-CDG, is an autosomal dominant O-linked glycosylation disorder characterized by the formation of multiple cartilage-capped tumors (osteochondromas). In contrast, solitary osteochondroma (SO) is a non-hereditary condition. EXT1 and EXT2, are tumor suppre...

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Detalles Bibliográficos
Autores principales: Delgado, M. A., Martinez-Domenech, G., Sarrión, P., Urreizti, R., Zecchini, L., Robledo, H. H., Segura, F., de Kremer, R. Dodelson, Balcells, S., Grinberg, D., Asteggiano, C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166712/
https://www.ncbi.nlm.nih.gov/pubmed/25230886
http://dx.doi.org/10.1038/srep06407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166712/
https://www.ncbi.nlm.nih.gov/pubmed/25230886
http://dx.doi.org/10.1038/srep06407

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