Electroclinical history of a five-year-old girl with GRIN1-related early-onset epileptic encephalopathy: a video-case study
نویسندگان
چکیده
منابع مشابه
GRIN1 Mutations in Early-Onset Epileptic Encephalopathy.
Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.
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ژورنال
عنوان ژورنال: Epileptic Disorders
سال: 2018
ISSN: 1294-9361,1950-6945
DOI: 10.1684/epd.2018.0992