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Publications by Jolien S. Klein Wassink-Ruiter

Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

American Journal of Human Genetics
Genetics
2019English

Novel Membrane Frizzled-Related Protein Gene Mutation as Cause of Posterior Microphthalmia Resulting in High Hyperopia With Macular Folds

Acta Ophthalmologica
MedicineOphthalmology
2013English

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