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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 - 2 (of 2 Records)

Query Trace: Disease Susceptibility and NIPA1[original query]
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Human molecular genetics 2010 Oct 19 (20): 4091-9.
Blauw Hylke M, Al-Chalabi Ammar, Andersen Peter M, van Vught Paul W J, Diekstra Frank P, van Es Michael A, Saris Christiaan G J, Groen Ewout J N, van Rheenen Wouter, Koppers Max, Van't Slot Ruben, Strengman Eric, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Uitterlinden Andre G, Kiemeney Lambertus A, Vermeulen Sita H M, Birve Anna, Waibel Stefan, Meyer Thomas, Cronin Simon, McLaughlin Russell L, Hardiman Orla, Sapp Peter C, Tobin Martin D, Wain Louise V, Tomik Barbara, Slowik Agnieszka, Lemmens Robin, Rujescu Dan, Schulte Claudia, Gasser Thomas, Brown Robert H, Landers John E, Robberecht Wim, Ludolph Albert C, Ophoff Roel A, Veldink Jan H, van den Berg Leonard
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.
Human molecular genetics 2012 Jun 21 (11): 2497-502.
Blauw Hylke M, van Rheenen Wouter, Koppers Max, Van Damme Philip, Waibel Stefan, Lemmens Robin, van Vught Paul W J, Meyer Thomas, Schulte Claudia, Gasser Thomas, Cuppen Edwin, Pasterkamp R Jeroen, Robberecht Wim, Ludolph Albert C, Veldink Jan H, van den Berg Leonard
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