Associated Papers
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC et al.
Nature Genetics, 2020
32989326 (PubMed )
Supplement: 41588_2020_695_MOESM3_ESM.xlsx › Data_set_1
Novel missense variants in the RNF213 gene from a European family with Moyamoya disease.
Gagunashvili AN et al.
Human Genome Variation, 2019
31645973 (PubMed )
Supplement: 41439_2019_66_MOESM1_ESM.pdf
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