ProfileOfResearchers

Identified 1

1

TITLE: A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy Full Text
AUTHORS: Mikko Muona; Samuel F Berkovic; Leanne M Dibbens; Karen L Oliver; Snezana Maljevic; Marta A Bayly; Tarja Joensuu; Laura Canafoglia; Silvana Franceschetti; Roberto Michelucci; Salla Markkinen; Sarah E Heron; Michael S Hildebrand; Eva Andermann; Frederick Andermann; Antonio Gambardella; Paolo Tinuper; Laura Licchetta; Ingrid E Scheffer; Chiara Criscuolo; Alessandro Filla; Edoardo Ferlazzo; Jamil Ahmad; Adeel Ahmad; Betul Baykan; Edith Said; Meral Topcu; Patrizia Riguzzi; Mary D King; Cigdem Ozkara; Danielle M Andrade; Bernt A Engelsen; Arielle Crespel; Matthias Lindenau; Ebba Lohmann; Veronica Saletti; João Massano ; Michael Privitera; Alberto J Espay; Birgit Kauffmann; Michael Duchowny; Rikke S Moller; Rachel Straussberg; Zaid Afawi; Bruria Ben Zeev; Kaitlin E Samocha; Mark J Daly; Steven Petrou; Holger Lerche; Aarno Palotie; Anna Elina Lehesjoki; ...More
PUBLISHED: 2015, SOURCE: NATURE GENETICS, VOLUME: 47, ISSUE: 1

INDEXED IN:

Scopus

WOS

© 2024 CRACS & Inesc TEC - All Rights Reserved Privacy Policy | Terms of Service