Cutaneous neurofibromas in the genomics era: current understanding and open questions

Cutaneous neurofibromas (cNF) are a nearly ubiquitous symptom of neurofibromatosis type 1 (NF1), a disorder with a broad phenotypic spectrum caused by germline mutation of the neurofibromatosis type 1 tumour suppressor gene (NF1). Symptoms of NF1 can include learning disabilities, bone abnormalities...

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Dades bibliogràfiques
Publicat a:Br J Cancer
Autors principals: Allaway, Robert J., Gosline, Sara J. C., La Rosa, Salvatore, Knight, Pamela, Bakker, Annette, Guinney, Justin, Le, Lu Q.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2018
Matèries:
Review Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6008439/
https://ncbi.nlm.nih.gov/pubmed/29695767
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41416-018-0073-2
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