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Exploring associations between constipation, severity of neurofibromatosis type 1 and NF1 mutational spectrum
Neurofibromatosis type 1 (NF1) is inherited in an autosomal dominant manner and is a rather common rare disease. Until recently, studies on gastrointestinal symptoms in patients with NF1 have been few and mostly described as case reports. In three previously published studies, the frequency of const...
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| Publicat a: | Sci Rep |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8080678/ https://ncbi.nlm.nih.gov/pubmed/33911094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-87686-x |
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