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Publications by Angela Brady
Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
American Journal of Human Genetics
Genetics
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy
American Journal of Human Genetics
Genetics
Refinement of the Locus for Hereditary Congenital Facial Palsy on Chromosome 3q21 in Two Unrelated Families and Screening of Positional Candidate Genes
European Journal of Human Genetics
Genetics