A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus.

Neuropediatrics

Clinical Genetics Unit, Department of Obstetrics and Pediatrics, Azienda Unità Sanitaria Locale, Arcispedale Santa Maria Nuova, IRCCS, Reggio Emilia, Italy.

Published: June 2018

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http://dx.doi.org/10.1055/s-0038-1641722DOI Listing

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