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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Detalles Bibliográficos
Autores principales: Allaway, Robert J., Gosline, Sara J. C., La Rosa, Salvatore, Knight, Pamela, Bakker, Annette, Guinney, Justin, Le, Lu Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008439/
https://www.ncbi.nlm.nih.gov/pubmed/29695767
http://dx.doi.org/10.1038/s41416-018-0073-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008439/
https://www.ncbi.nlm.nih.gov/pubmed/29695767
http://dx.doi.org/10.1038/s41416-018-0073-2

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