Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Blepharospasm, Oromandibular Dystonia, and Meige Syndrome: Clinical and Genetic Update.
Ma H et al.
Frontiers in Neurology, 2021
Whole-exome sequencing for variant discovery in blepharospasm.
Tian J et al.
Molecular Genetics & Genomic Medicine, 2018
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