Associated Papers
Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.
Liu Y et al.
Molecular Cancer, 2023
37543594 (PubMed )
Supplement: 12943_2023_1828_MOESM2_ESM.xlsx › supplementaryTable_1B
Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus-dystonia.
Chbel F et al.
Clinical Case Reports, 2022
Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome.
Rachad L et al.
Neuroscience Letters, 2019
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