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Publications by Keren J. Carss
Bi-Allelic Loss-Of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia
American Journal of Human Genetics
Genetics
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias
American Journal of Human Genetics
Genetics
Unique Non-Coding Variants Upstream of PRDM13 Are Associated With a Spectrum of Developmental Retinal Dystrophies Including Progressive Bifocal Chorioretinal Atrophy
Human Mutation
Genetics
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