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Publications by Simon Holden

Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

American Journal of Human Genetics

English

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American Journal of Human Genetics

English

A Case-Note Review of Continued Pregnancies Found to Be at a High Risk of Huntington’s Disease: Considerations for Clinical Practice

European Journal of Human Genetics

English