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Genetic studies of amyotrophic lateral sclerosis: Controversies and perspectives

期刊

AMYOTROPHIC LATERAL SCLEROSIS
卷 10, 期 1, 页码 1-14

出版社

INFORMA HEALTHCARE
DOI: 10.1080/17482960802585469

关键词

Genetics; association; linkage; genome-wide association; copy number variation

资金

  1. Motor Neurone Disease Association and the Medical Research Council
  2. Medical Research Council [G0600974] Funding Source: researchfish
  3. MRC [G0600974] Funding Source: UKRI

向作者/读者索取更多资源

The genetic causes of amyotrophic lateral sclerosis (ALS) are slowly being dissected out with the help of recent advances in genetic technology. Linkage studies and association studies examining candidate genes, candidate pathways, and genome-wide association have been used, based on direct sequencing and correlations between genetic variations. Copy number and microsatellite variants have also been examined, although the ideal methods for analysis are still being developed. In this review we examine the evidence for a genetic basis to ALS, discuss the challenges and difficulties faced and summarize the support for the reported genetic causes of ALS.

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