Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.
第一作者:
Heather E,Olson
第一单位:
Epilepsy Genetics Program, Department of Neurology, Division of Epilepsy and Clinical Neurophysiology, Boston Children's Hospital, Boston, MA.;Harvard Medical School, Boston, MA.
作者:
医学主题词
青少年(Adolescent);氨酰基tRNA合成酶类(Amino Acyl-tRNA Synthetases);儿童(Child);儿童, 学龄前(Child, Preschool);脑电描记术(Electroencephalography);女(雌)性(Female);随访研究(Follow-Up Studies);基因检测(Genetic Testing);基因型(Genotype);人类(Humans);婴儿(Infant);婴儿, 新生(Infant, Newborn);KCNQ2钾通道(KCNQ2 Potassium Channel);磁共振成像(Magnetic Resonance Imaging);男(雄)性(Male);表型(Phenotype);痉挛, 婴儿(Spasms, Infantile)
DOI
10.1002/ana.24883
PMID
28133863
发布时间
2019-04-01
- 浏览13
Annals of neurology
419-429页
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