Associated Papers
Further delineation of the SCAF4-associated neurodevelopmental disorder.
Schmid CM et al.
European Journal of Human Genetics : Ejhg, 2025
39668183 (PubMed )
Supplement: 41431_2024_1760_MOESM1_ESM.xlsx › Supplement_S1
Understanding rare variant contributions to autism: lessons from dystrophin-deficient model.
Costa CIS et al.
Npj Genomic Medicine, 2025
A novel nonsense mutation in SCAF4 associated with fliedner-zweier syndrome: a case report and review of the literature.
Chen Z et al.
Frontiers in Genetics, 2025
40290495 (PubMed )
Supplement: Table1.xlsx › Sheet1
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