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Query Trace: Amyotrophic Lateral Sclerosis and HTT[original query]

Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics. Journal of the neurological sciences 2019 May 402 62-68. Goldstein Orly, Kedmi Merav, Gana-Weisz Mali, Twito Shir, Nefussy Beatrice, Vainer Batel, Fainmesser Yaara, Abraham Alon, Nayshool Omri, Orr-Urtreger Avi, Drory Vivian Similar articles in PubMed
Defining neurodegeneration on Guam by targeted genomic sequencing. Annals of neurology 2015 Mar 77 (3): 458-68. Steele John C, Guella Ilaria, Szu-Tu Chelsea, Lin Michelle K, Thompson Christina, Evans Daniel M, Sherman Holly E, Vilariño-Güell Carles, Gwinn Katrina, Morris Huw, Dickson Dennis W, Farrer Matthew Similar articles in PubMed
Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 May 13 (3): 265-9. Ramos Eliana Marisa, Keagle Pamela, Gillis Tammy, Lowe Patrick, Mysore Jayalakshmi S, Leclerc Ashley Lyn, Ratti Antonia, Ticozzi Nicola, Gellera Cinzia, Gusella James F, Silani Vincenzo, Alonso Isabel, Brown Robert H, MacDonald Marcy E, Landers John Similar articles in PubMed