| Literature DB >> 29103041 |
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.Entities:
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