Article (Scientific journals)
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality
Bailey, JN; Patterson, C; de Nijs, L et al.
2017In Genetics in Medicine, 19, p. 144-156
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Disciplines :
Neurology
Author, co-author :
Bailey, JN 
Patterson, C 
de Nijs, L
Duron, RM
Ngyen, VH
Tanaka, M
Medina, MT
Jara-Prado, A
Martinez-Juarez, IE
Ochoa, A
Molina, Y
Suzuki, T
Alonso, ME
Wight, JE
Lin, YC
Guilhoto, L
Yacubian, EMT
Machado-Salas, J
Daga, A
Yamakawa, K
Grisar, Thierry ;  Université de Liège > Département des sciences biomédicales et précliniques > Département des sciences biomédicales et précliniques
Lakaye, Bernard ;  Université de Liège > Département des sciences biomédicales et précliniques > Biochimie et physiologie humaine et pathologique
Delgado-Escueta, AV
More authors (13 more) Less
 These authors have contributed equally to this work.
Language :
English
Title :
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality
Publication date :
2017
Journal title :
Genetics in Medicine
ISSN :
1098-3600
eISSN :
1530-0366
Publisher :
Lippincott Williams & Wilkins, United States
Volume :
19
Pages :
144-156
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 19 January 2017

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