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Case Reports in Genetics
Volume 2019, Article ID 9650184, 5 pages
https://doi.org/10.1155/2019/9650184
Case Series

Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome

1Department of Plastic Surgery, Hospital South West Jutland, Esbjerg, Denmark
2Department of Dermatology and Allergy, Gentofte Hospital and Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
3Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
4Department of Plastic Surgery and Burns Treatment, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
5Department of Clinical Genetics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Correspondence should be addressed to Gustav Askaner; moc.liamg@renaksag

Received 1 May 2019; Revised 13 June 2019; Accepted 1 July 2019; Published 28 July 2019

Academic Editor: Christos Yapijakis

Copyright © 2019 Gustav Askaner et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Gustav Askaner, Ulrikke Lei, Birgitte Bertelsen, Alessandro Venzo, and Karin Wadt, “Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome,” Case Reports in Genetics, vol. 2019, Article ID 9650184, 5 pages, 2019. https://doi.org/10.1155/2019/9650184.