Associated Papers
Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families.
AlAbdi L et al.
Nature Communications, 2023
37644014 (PubMed )
Supplement: 41467_2023_40909_MOESM10_ESM.xlsx › Sheet1
RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability.
Scala M et al.
Brain : a Journal of Neurology, 2020
GWAS signals revisited using human knockouts.
Maddirevula S et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
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