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Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
Segmental progeroid syndromes are commonly represented by genetic conditions which recapitulate aspects of physiological aging by similar, disparate, or unknown mechanisms. Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease caused by mutations in the gene for ACVR1/ALK2 encoding A...
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| Udgivet i: | Front Endocrinol (Lausanne) |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Frontiers Media S.A.
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6966325/ https://ncbi.nlm.nih.gov/pubmed/31998237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2019.00908 |
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