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Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966
Neurofibromatosis type 1 is a relatively common genetic disease, with a prevalence ranging between 1/3000 and 1/6000 people worldwide. The disease affects multiple systems with cutaneous, neurologic, and orthopedic as major manifestations which lead to significant morbidity or mortality. Indeed, NF1...
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| Publicado no: | Orphanet J Rare Dis |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6998847/ https://ncbi.nlm.nih.gov/pubmed/32014052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1310-3 |
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