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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and MATR3[original query]
Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients.
Neurobiology of aging 2014 Dec 35 (12): 2882.e13-5.
Millecamps Stéphanie, De Septenville Anne, Teyssou Elisa, Daniau Mailys, Camuzat Agnès, Albert Mélanie, LeGuern Eric, Galimberti Daniela, , Brice Alexis, Marie Yannick, Le Ber Isabel
Mutation analysis of MATR3 in Australian familial amyotrophic lateral sclerosis.
Neurobiology of aging 2015 Mar 36 (3): 1602.e1-2.
Fifita Jennifer A, Williams Kelly L, McCann Emily P, O'Brien Aidan, Bauer Denis C, Nicholson Garth A, Blair Ian
ALS Genes in the Genomic Era and their Implications for FTD.
Trends in genetics : TIG 2018 4 34 (6): 404-423.
Nguyen Hung Phuoc, Van Broeckhoven Christine, van der Zee Jul
Comprehensive Genetic Analysis of a Hungarian Amyotrophic Lateral Sclerosis Cohort.
Frontiers in genetics 2019 10 732.
Tripolszki Kornélia, Gampawar Piyush, Schmidt Helena, Nagy Zsófia F, Nagy Dóra, Klivényi Péter, Engelhardt József I, Széll Már
Role of MAPT in Pure Motor Neuron Disease: Report of a Recurrent Mutation in Italian Patients.
Neuro-degenerative diseases 2019 Mar 18 (5-6): 310-314.
Origone Paola, Geroldi Alessandro, Lamp Merit, Sanguineri Francesca, Caponnetto Claudia, Cabona Corrado, Gotta Fabio, Trevisan Lucia, Bellone Emilia, Manganelli Fiore, Devigili Grazia, Mandich Pao
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