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Inherited pulmonary cylindromas: extending the phenotype of CYLD mutation carriers
BACKGROUND: Germline mutations in the tumour suppressor gene CYLD are recognized to be associated with the development of multiple cutaneous cylindromas. We encountered such a patient who presented with breathlessness because of multiple pulmonary cylindromas. OBJECTIVES: To search for clinical and...
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| Publicado no: | Br J Dermatol |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6175122/ https://ncbi.nlm.nih.gov/pubmed/29569226 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjd.16573 |
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