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

I. Maini, E. Farnetti, S. G. Caraffi, I. Ivanovski, M. L. de Bernardi, C. Gelmini, M. Pollazzon, S. Rosato, S. Laurie, L. Matalonga, C. Baldo, L. Garavelli

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Publication statusAccepted/In press - Apr 11 2018

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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