Literature DB >> 29103041

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline.

Irene Piaceri1, Valentina Bessi2, Sabrina Matà2, Cristina Polito3, Andrea Tedde1, Valentina Berti3, Silvia Bagnoli1, Arianna Braccia1, Monica Del Mastio2, Alberto Moggi Pignone4, Alberto Pupi3, Sandro Sorbi1,2,5, Benedetta Nacmias1.   

Abstract

A new risk gene associated with amyotrophic lateral sclerosis (ALS) has recently been identified: the Tank-binding kinase 1 (TBK1) gene. Up to now, 90 TBK1 variants have been described in ALS patients with or without frontotemporal dementia (FTD), thus making TBK1 the third or fourth most frequent genetic cause of ALS and FTD. A point mutation analysis in a cohort of 69 Italian ALS patients was performed in order to analyze the frequency of TBK1 mutations and the correlation with clinical phenotypes. The analysis identified the novel variant p.Tyr424Asp in a patient with a rapid progression of the disease. Our data supports the implication of TBK1 in ALS pathogenesis in Italy.

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Keywords:  Amyotrophic lateral sclerosis; Italy; genetics; missense mutation

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Year:  2018        PMID: 29103041     DOI: 10.3233/JAD-170694

Source DB:  PubMed          Journal:  J Alzheimers Dis        ISSN: 1387-2877            Impact factor:   4.472


  1 in total

Review 1.  Association of the TBK1 mutation p.Ile334Thr with frontotemporal dementia and literature review.

Authors:  Huiling Yu; Wenbo Yu; Su-Shan Luo; Yu-Jie Yang; Feng-Tao Liu; Yue Zhang; Yan Chen; Yi-Min Sun; Jian-Jun Wu
Journal:  Mol Genet Genomic Med       Date:  2019-01-22       Impact factor: 2.183

  1 in total

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