PRRT2 mutation in Japanese children with benign infantile epilepsy

Brain and Development

Volumn 35, Issue 7, 2013, Pages 641-646

  Okumura, Akihisa ^a   Shimojima, Keiko ^b   Kubota, Tetsuo ^c   Abe, Shinpei ^a   Yamashita, Shintaro ^d   Imai, Katsumi ^e   Okanishi, Tohru ^f   Enoki, Hideo ^f   Fukasawa, Tatsuya ^c   Tanabe, Takuya ^g   Dibbens, Leanne M ^h   Shimizu, Toshiaki ^a   Yamamoto, Toshiyuki ^b  

^a JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^c ANJO KOSEI HOSPITAL   (Japan)

^d JUNTENDO UNIVERSITY NERIMA HOSPITAL   (Japan)

^e SHIZUOKA INSTITUTE OF EPILEPSY AND NEUROLOGICAL DISORDERS   (Japan)

^f SEIREI HAMAMATSU GENERAL HOSPITAL   (Japan)

^g Tanabe Children's Clinic   (Japan)

^h UNIVERSITY OF SOUTH AUSTRALIA   (Australia)

Author keywords

Benign infantile epilepsy; Japanese children; Paroxysmal kinesigenic dyskinesia; PRRT2

Indexed keywords

ANTICONVULSIVE AGENT;

AMINO ACID SEQUENCE; ARTICLE; BENIGN INFANTILE EPILEPSY; CHILD; CLINICAL ARTICLE; CONVULSION; EPILEPSY; FAMILY HISTORY; FEMALE; GASTROENTERITIS; GENE; GENE MUTATION; HUMAN; JAPANESE; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PAROXYSMAL KINESIGENIC DYSKINESIA; PEDIGREE ANALYSIS; PRESCHOOL CHILD; PRRT2 GENE; SCHOOL CHILD; SEIZURE;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHOREA; DNA MUTATIONAL ANALYSIS; EPILEPSY, BENIGN NEONATAL; FEMALE; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION; NERVE TISSUE PROTEINS; PEDIGREE; POLYMERASE CHAIN REACTION;

EID: 84879462687     PISSN: 03877604     EISSN: 18727131     Source Type: Journal    
DOI: 10.1016/j.braindev.2012.09.015     Document Type: Article

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