Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.

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作者： Benjamin,Gaastra ^[1] ; Aleksey,Shatunov ^[1] ; Sara,Pulit ^[2] ; Ashley R,Jones ^[1] ; William,Sproviero ^[1] ; Alexandra,Gillett ^[3] ; Zhongbo,Chen ^[1] ; Janine,Kirby ^[4] ; Isabella,Fogh ^[1] ; John F,Powell ^[1] ; P Nigel,Leigh ^[5] ; Karen E,Morrison ^[6] ; Pamela J,Shaw ^[4] ; Christopher E,Shaw ^[1] ; Leonard H,van den Berg ^[2] ; Jan H,Veldink ^[2] ; Cathryn M,Lewis ^[3] ; Ammar,Al-Chalabi ^[1]

作者单位： a Maurice Wohl Clinical Neuroscience Institute, King's College London, Institute of Psychiatry, Psychology and Neuroscience , London , UK. ^[1] b University Medical Centre Utrecht , Utrecht , The Netherlands. ^[2] c Department of Statistical Genetics, King's College London , Institute of Psychiatry, Psychology and Neuroscience , London, UK. ^[3] d Sheffield Institute for Translational Neuroscience , Sheffield, UK. ^[4] e Brighton and Sussex Medical School , Brighton, UK , and. ^[5] f Faculty of Medicine , University of Southampton , Southampton , UK. ^[6]

关键词 ALS UNC13A genetic modifiers sequencing survival

主题词衔接蛋白质类, 信号转导(Adaptor Proteins, Signal Transducing);肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis);队列研究(Cohort Studies);细胞支架蛋白质类(Cytoskeletal Proteins);数据库, 文献型(Databases, Bibliographic);女(雌)性(Female);基因型(Genotype);人类(Humans);男(雄)性(Male);中年人(Middle Aged);神经组织蛋白质类(Nerve Tissue Proteins);多态性, 单核苷酸(Polymorphism, Single Nucleotide);受体, EphA4(Receptor, EphA4);存活率分析(Survival Analysis);时间因素(Time Factors)

DOI 10.1080/21678421.2016.1213852

PMID 27584932

发布时间 2024-03-20

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Amyotrophic lateral sclerosis & frontotemporal degeneration

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Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.

Amyotrophic lateral sclerosis & frontotemporal degeneration

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Amyotrophic lateral sclerosis & frontotemporal degeneration

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Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.

Amyotrophic lateral sclerosis & frontotemporal degeneration

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Amyotrophic lateral sclerosis & frontotemporal degeneration

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