Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.
第一作者:
Kerstin U,Ludwig
第一单位:
Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.;Institute of Human Genetics, University of Bonn, Bonn, Germany.
作者:
医学主题词
成年人(Adult);注意力缺陷障碍伴多动(Attention Deficit Disorder with Hyperactivity);儿童(Child);认知障碍(Cognition Disorders);共病现象(Comorbidity);阅读障碍(Dyslexia);女(雌)性(Female);遗传变异(Genetic Variation);单倍型(Haplotypes);人类(Humans);语言(Language);男(雄)性(Male);记忆, 短时(Memory, Short-Term);阅读(Reading);受体, N-甲基-D-天冬氨酸(Receptors, N-Methyl-D-Aspartate)
DOI
10.1002/ajmg.b.31007
PMID
19591125
发布时间
2020-09-30
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