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dc.contributor.authorDiekstra, F
dc.contributor.authorVan, E S M
dc.contributor.authorEstrada, K
dc.contributor.authorRivadeneira, F
dc.contributor.authorHofman, A
dc.contributor.authorUitterlinden, A
dc.contributor.authorRobberecht, W
dc.contributor.authorAndersen, P
dc.contributor.authorMelki, J
dc.contributor.authorMeininger, V
dc.contributor.authorHardiman, O
dc.contributor.authorLanders, J
dc.contributor.authorBrown, J R R
dc.contributor.authorShatunov, A
dc.contributor.authorAl-Chalabi, A
dc.contributor.authorChio, A
dc.contributor.authorDegenerati, N
dc.contributor.authorVan Swieten, J
dc.contributor.authorVan Den Berg, L
dc.contributor.authorVeldink, J
dc.date.accessioned2012-08-16T10:13:29Z
dc.date.available2012-08-16T10:13:29Z
dc.date.issued2011-11
dc.identifier.citationAmyotrophic Lateral Sclerosis (2011) 12 SUPPL. 1 (36). : November 2011en_GB
dc.identifier.urihttp://hdl.handle.net/10147/238971
dc.language.isoenen
dc.titleCombined genome-wide analysis identifies UNC13A and chromosome 9P21.1 as shared loci for susceptibility to amyotrophic lateral sclerosis and frontotemporal lobar degenerationen_GB
dc.typeConference Presentationen
dc.description.provinceLeinsteren


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