Clinical and Genetic Study of the First Japanese FTDP-17 Patient with a Mutation of +3 in Intron 10 in the MAPT Gene.

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作者： Haitian,Nan ^[1] ; Ryusuke,Takaki ^[2] ; Keisuke,Shimozono ^[1] ; Yuta,Ichinose ^[1] ; Kishin,Koh ^[1] ; Yoshihisa,Takiyama ^[1]

作者单位： Department of Neurology, Graduate School of Medical Sciences, University of Yamanashi, Japan. ^[1] Department of Neurology, Iida Hospital, Japan. ^[2]

关键词 FTDP-17 H1M haplotype IVS10+3G>A mutation MAPT non-Caucasian

主题词成年人(Adult);老年人(Aged);老年人, 80以上(Aged, 80 and over);染色体, 人, 17对(Chromosomes, Human, Pair 17);家庭(Family);女(雌)性(Female);额颞叶痴呆(Frontotemporal Dementia);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);日本(Japan);男(雄)性(Male);中年人(Middle Aged);突变(Mutation);帕金森障碍(Parkinsonian Disorders);表型(Phenotype);tau蛋白质类(tau Proteins)

DOI 10.2169/internalmedicine.2761-19

PMID 30996196

发布时间 2020-02-25

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Internal medicine (Tokyo, Japan)

2019年58卷16期

2397-2400页

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Clinical and Genetic Study of the First Japanese FTDP-17 Patient with a Mutation of +3 in Intron 10 in the MAPT Gene.

Internal medicine (Tokyo, Japan)

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Internal medicine (Tokyo, Japan)

相关期刊

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Clinical and Genetic Study of the First Japanese FTDP-17 Patient with a Mutation of +3 in Intron 10 in the MAPT Gene.

Internal medicine (Tokyo, Japan)

相似文献

Internal medicine (Tokyo, Japan)

相关期刊

检索历史清除