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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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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4166712/ https://ncbi.nlm.nih.gov/pubmed/25230886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep06407 |
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