A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Blauw HM; Al-Chalabi A; Andersen PM; van Vught PW; Diekstra FP; van Es MA; Saris CG; Groen EJ; van Rheenen W; Koppers M; Van't Slot R; Strengman E; Estrada K; Rivadeneira F; Hofman A; Uitterlinden AG; Kiemeney LA; Vermeulen SH; Birve A; Waibel S; Meyer T; Cronin S; McLaughlin RL; Hardiman O; Sapp PC; Tobin MD; Wain LV; Tomik B; Slowik A; Lemmens R; Rujescu D; Schulte C; Gasser T; Brown RH Jr; Landers JE; Robberecht W; Ludolph AC; Ophoff RA; Veldink JH; van den Berg LH; Human Molecular Genetics, 2010, vol. 19, issue 20, p 4091, ISSN 14602083. ISBN 14602083.

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