摘要
在过去二十年里,神经遗传的快速发展不仅在分子,病理,遗传方面,也在肌萎缩侧索硬化(ALS)的临床概念上发生了改变。 在这里,我们回顾了遗传性和散发性ALS中当前的遗传突破,并考虑到如何使得这些知识在可能的遗传疾病机制方案的拓展和更好的了解遗传、病理及临床亚型之间的关系。
关键词: 肌萎缩侧索硬化,痴呆,基因测试,全基因组关联,突变,表型,WES
Current Molecular Medicine
Title:Amyotrophic Lateral Sclerosis: A Genetic Point of View
Volume: 14 Issue: 8
Author(s): C. Carlesi, E. Caldarazzo Ienco, M. Mancuso and G. Siciliano
Affiliation:
关键词: 肌萎缩侧索硬化,痴呆,基因测试,全基因组关联,突变,表型,WES
摘要: In the last twenty years the rapid advances in neurogenetic have revolutionized not only the molecular, pathological, inheritance but also the clinical concept of ALS.
Here we review the current genetic breakthrough in familial and sporadic ALS, considering how this knowledge has allowed widening of the scenario on the possible pathogenic disease mechanisms and better understanding of the relationship between the genetic, pathological and clinical subtypes.
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Cite this article as:
Carlesi C., Ienco Caldarazzo E., Mancuso M. and Siciliano G., Amyotrophic Lateral Sclerosis: A Genetic Point of View, Current Molecular Medicine 2014; 14 (8) . https://dx.doi.org/10.2174/1566524014666141010155822
DOI https://dx.doi.org/10.2174/1566524014666141010155822 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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