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Publications by Louise Ocaka

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

American Journal of Human Genetics
Genetics
2015English

Novel Missense Variants in the RNF213 Gene From a European Family With Moyamoya Disease

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2019English

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