Julien Buratti
Hôpital Universitaire Pitié Salpêtrière
9 papers found
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The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant
UploadBiallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
UploadAuthor Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Download from www.nature.comMutations disrupting neuritogenesis genes confer risk for cerebral palsy
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