Associated Papers
Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.
Guerrini-Rousseau L et al.
Journal of Medical Genetics, 2022
35768194 (PubMed )
Supplement: jmedgenet-2021-108385supp005.pdf
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia.
Schröder S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Novel SUFU Frameshift Variant Leading to Meningioma in Three Generations in a Family with Gorlin Syndrome.
Askaner G et al.
Case Reports in Genetics, 2019
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