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Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout

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作者： Magri, Stefania ^[1] ; Nanetti, Lorenzo ; Mongelli, Alessia ; Rizzo, Elena ; Taroni, Franco ; Mariotti, Caterina ; Gellera, Cinzia

作者单位： Fdn IRCCS Ist Neurol Carlo Besta, Dept Diagnost & Technol, Unit Med Genet & Neurogenet, Milan, Italy ^[1]

关键词 allele dropout CAG triplet chorea Huntington disease

发布时间 2021-04-09

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American journal of medical genetics, Part A

2021年185A卷2期

397-400页

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American journal of medical genetics, Part A

2021年185A卷2期

397-400页

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Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout

American journal of medical genetics, Part A

相似文献

American journal of medical genetics, Part A

相关期刊

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Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout

American journal of medical genetics, Part A

相似文献

American journal of medical genetics, Part A

相关期刊

检索历史清除