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Lookup NU author(s): Dr Neil RajanORCiD
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
This article is protected by copyright. All rights reserved.The tumours arising in naevoid basal cell carcinoma syndrome (NBCCS) and neurofibromatosis type 1 (NF1) are distinct, and are exemplars of the specific consequences of mutations arising in different tumour suppressor genes. Whilst each syndrome has recognised pathognomonic tumours, an exceptional spectrum of tumours presenting in an individual with either syndrome may represent the interaction of an additional tumour suppressor gene.
Author(s): Ghadiri SJ, Brennan P, Calonje E, Carmichael AJ, Rajan N
Publication type: Letter
Publication status: Published
Journal: The British Journal of Dermatology
Print publication date: 01/12/2020
Online publication date: 20/06/2020
Acceptance date: 10/06/2020
ISSN (print): 0007-0963
ISSN (electronic): 1365-2133
Publisher: NLM (Medline)
PubMed id: 32562549