Open AccessA clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental retardation, autism, and movement disorders
Author(s) -
M. Yu. Bobylova,
М. Б. Миронов,
А. В. Куликов,
Maria Kazakova,
M.A. Bogacheva,
Yu.A. Tankevich,
L. Yu . Glukhova,
Е. И. Барлетова,
М. О. Абрамов,
К. Yu. Mukhin,
G. E. Rudenskaya
Publication year - 2014
Publication title -
nevrologiâ, nejropsihiatriâ, psihosomatika
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.157
H-Index - 9
eISSN - 2310-1342
pISSN - 2074-2711
DOI - 10.14412/2074-2711-2014-2-34-40
Subject(s) - autism , epilepsy , psychology , psychiatry , comorbidity , developmental disorder , medicine , pediatrics , clinical psychology