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Publications by Dennis Lal

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

English

Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

American Journal of Human Genetics

English

Clinical Spectrum of STX1B-related Epileptic Disorders

English

Delineating the GRIN1 Phenotypic Spectrum

English

Functional Interpretation of Single Amino Acid Substitutions in 1,330 Disease-Associated Genes

Biophysical Journal

English

The Contribution of CACNA1A, ATP1A2 and SCN1A Mutations in Hemiplegic Migraine: A Clinical and Genetic Study in Finnish Migraine Families

English