De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin Journal Articles Refereed uri icon

Overview

Published in

  • Journal of Medical Genetics

Time

Date/time value

  • 2010

Identity

Digital Object Identifier (DOI)

  • 10.1136/jmg.2008.065912

Additional Document Info

Parent Title

  • JOURNAL OF MEDICAL GENETICS

Volume

  • 47

Issue

  • 2

Publisher

  • BMJ Publishing Group