TY  - GEN
AU  - Tsuchida,N
AU  - Nakashima,M
AU  - Kato,M
AU  - Heyman,E
AU  - Inui,T
AU  - Haginoya,K
AU  - Watanabe,S
AU  - Chiyonobu,T
AU  - Morimoto,M
AU  - Ohta,M
AU  - Kumakura,A
AU  - Kubota,M
AU  - Kumagai,Y
AU  - Hamano,S-I
AU  - Lourenco,C M
AU  - Yahaya,N A
AU  - Ch'ng,G-S
AU  - Ngu,L-H
AU  - Fattal-Valevski,A
AU  - Weisz Hubshman,M
AU  - Orenstein,N
AU  - Marom,D
AU  - Cohen,L
AU  - Goldberg-Stern,H
AU  - Uchiyama,Y
AU  - Imagawa,E
AU  - Mizuguchi,T
AU  - Takata,A
AU  - Miyake,N
AU  - Nakajima,H
AU  - Saitsu,H
AU  - Miyatake,S
AU  - Matsumoto,N
TI  - Detection of copy number variations in epilepsy using exome data
SN  - 1399-0004
PY  - 2019///0911
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Alleles
KW  - Child
KW  - Child, Preschool
KW  - Comparative Genomic Hybridization
KW  - Computational Biology
KW  - methods
KW  - DNA Copy Number Variations
KW  - Epilepsy
KW  - diagnosis
KW  - Exome
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Exome Sequencing
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/cge.13144
ER  -