Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and STMN2[original query] |
---|
Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 8 8 (4): e678. Ross Jay P, Akçimen Fulya, Liao Calwing, Spiegelman Dan, Weisburd Ben, Dupré Nicolas, Dion Patrick A, Rouleau Guy A, Farhan Sali M |
Analysis of STMN2 CA repeats in italian ALS patients shows no association. Amyotrophic lateral sclerosis & frontotemporal degeneration 2022 Jul 1-3. Doronzio Paolo Niccolò, Lattante Serena, Marangi Giuseppe, Martello Francesco, Conte Amelia, Bisogni Giulia, Bernardo Daniela, Patanella Agata Katia, Meleo Emiliana, Zollino Marcella, Sabatelli Mar |
NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk. Neurobiology of aging 2022 Aug 116 92-95. Grima Natalie, Henden Lyndal, Fearnley Liam G, Rowe Dominic B, D'Silva Susan, Pamphlett Roger, Adams Lorel, Kiernan Matthew C, Mazumder Srestha, Timmins Hannah C, Zoing Margaret, Bahlo Melanie, Blair Ian P, Williams Kelly |
Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans. Neurology. Genetics 2023 6 9 (4): e200077. Nomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, Gerrit Botha, Nicola J Mulder, Gang Wu, Evadnie Rampersaud, Jason Myers, Marka Van Blitterswijk, Rosa Rademakers, J Paul Taylor, Joanne Wuu, Michael Benatar, Melissa N |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 13, 2024
- Content source: