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Your search keyword '"Peeters, Els A. J."' showing total 3 results

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1. Recurrent KIF2A mutations are responsible for classic lissencephaly

2. Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

3. Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

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