Record title
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Record identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4281260
Record permalink
https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4281260
Share
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
About this item
Full title
Author / Creator
Publisher
United States: Nature Publishing Group
Journal title
Record Identifier
Language
English
Formats
Publication information
Publisher
Subjects
More information
Scope and Contents
Contents
Alternative Titles
Full title
Authors, Artists and Contributors
Author / Creator
Berkovic, Samuel F
Dibbens, Leanne M
Oliver, Karen L
Maljevic, Snezana
Bayly, Marta A
Joensuu, Tarja
Canafoglia, Laura
Franceschetti, Silvana
Michelucci, Roberto
Markkinen, Salla
Heron, Sarah E
Hildebrand, Michael S
Andermann, Eva
Andermann, Frederick
Gambardella, Antonio
Tinuper, Paolo
Licchetta, Laura
Scheffer, Ingrid E
Criscuolo, Chiara
Filla, Alessandro
Ferlazzo, Edoardo
Ahmad, Jamil
Ahmad, Adeel
Baykan, Betul
Said, Edith
Topcu, Meral
Riguzzi, Patrizia
King, Mary D
Ozkara, Cigdem
Andrade, Danielle M
Engelsen, Bernt A
Crespel, Arielle
Lindenau, Matthias
Lohmann, Ebba
Saletti, Veronica
Massano, João
Privitera, Michael
Espay, Alberto J
Kauffmann, Birgit
Duchowny, Michael
Møller, Rikke S
Straussberg, Rachel
Afawi, Zaid
Ben-Zeev, Bruria
Samocha, Kaitlin E
Daly, Mark J
Petrou, Steven
Lerche, Holger
Palotie, Aarno
Lehesjoki, Anna-Elina
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4281260
Permalink
https://collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4281260
Other Identifiers
ISSN
E-ISSN
DOI