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Updated: Jul 5, 2025

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
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在C9orf72六核酸重复扩张和中长度等位基因之间的共同祖先使用了哈普罗型共享树和HAPTK

Osma S Rautila1, Karri Kaivola1, Harri Rautila2

  • 1Translational Immunology, Research Programs Unit, University of Helsinki, Helsinki, Finland; Department of Neurology, Helsinki University Hospital, Helsinki, Finland.

American journal of human genetics
|January 19, 2024
PubMed
概括

C9orf72六核酸重复扩张 (HRE) 是ALS和FTD的关键遗传原因. 较长的中间长度等位基因 (IAs) 与HRE共享广泛的单位基因类型,这表明它们可能是潜在的前变异等位基因.

关键词:
这就是ALS.C9orf7272 是一个很好的方法.这是一个FTD.GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC GGGGCC这是一个哈普特克.在HST上,HST就是HST.哈普罗类型共享树的树.重复的疾病是重复的疾病.重复扩张的扩张.

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