Search: onr:"swepub:oai:DiVA.org:umu-42297" > Chromosome 9p21 in ...
Fältnamn | Indikatorer | Metadata |
---|---|---|
000 | 02864naa a2200685 4500 | |
001 | oai:DiVA.org:umu-42297 | |
003 | SwePub | |
008 | 110407s2010 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-422972 URI |
024 | 7 | a https://doi.org/10.1016/S1474-4422(10)70197-62 DOI |
040 | a (SwePub)umu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Shatunov, Aleksey4 aut |
245 | 1 0 | a Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries :b a genome-wide association study |
264 | 1 | c 2010 |
338 | a print2 rdacarrier | |
520 | a We have found strong evidence of a genetic association of two single nucleotide polymorphisms on chromosome 9 with sporadic ALS, in line with findings from previous independent GWAS of ALS and linkage studies of ALS-frontotemporal dementia. Our findings together with these earlier findings suggest that genetic variation at this locus on chromosome 9 causes sporadic ALS and familial ALS-frontotemporal dementia. Resequencing studies and then functional analysis should be done to identify the defective gene. | |
700 | 1 | a Mok, Kin4 aut |
700 | 1 | a Newhouse, Stephen4 aut |
700 | 1 | a Weale, Michael E4 aut |
700 | 1 | a Smith, Bradley4 aut |
700 | 1 | a Vance, Caroline4 aut |
700 | 1 | a Johnson, Lauren4 aut |
700 | 1 | a Veldink, Jan H4 aut |
700 | 1 | a van Es, Michael A4 aut |
700 | 1 | a van den Berg, Leonard H4 aut |
700 | 1 | a Robberecht, Wim4 aut |
700 | 1 | a Van Damme, Philip4 aut |
700 | 1 | a Hardiman, Orla4 aut |
700 | 1 | a Farmer, Anne E4 aut |
700 | 1 | a Lewis, Cathryn M4 aut |
700 | 1 | a Butler, Amy W4 aut |
700 | 1 | a Abel, Olubunmi4 aut |
700 | 1 | a Andersen, Peter Mu Umeå universitet,Neurologi4 aut0 (Swepub:umu)pean0001 |
700 | 1 | a Fogh, Isabella4 aut |
700 | 1 | a Silani, Vincenzo4 aut |
700 | 1 | a Chiò, Adriano4 aut |
700 | 1 | a Traynor, Bryan J4 aut |
700 | 1 | a Melki, Judith4 aut |
700 | 1 | a Meininger, Vincent4 aut |
700 | 1 | a Landers, John E4 aut |
700 | 1 | a McGuffin, Peter4 aut |
700 | 1 | a Glass, Jonathan D4 aut |
700 | 1 | a Pall, Hardev4 aut |
700 | 1 | a Leigh, P Nigel4 aut |
700 | 1 | a Hardy, John4 aut |
700 | 1 | a Brown, Robert H4 aut |
700 | 1 | a Powell, John F4 aut |
700 | 1 | a Orrell, Richard W4 aut |
700 | 1 | a Morrison, Karen E4 aut |
700 | 1 | a Shaw, Pamela J4 aut |
700 | 1 | a Shaw, Christopher E4 aut |
700 | 1 | a Al-Chalabi, Ammar4 aut |
710 | 2 | a Umeå universitetb Neurologi4 org |
773 | 0 | t Lancet Neurologyg 9:10, s. 986-994q 9:10<986-994x 1474-4422x 1474-4465 |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-42297 |
856 | 4 8 | u https://doi.org/10.1016/S1474-4422(10)70197-6 |
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