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Autor:
Ababneh, N
The hexanucleotide repeat expansion (HRE) mutation within C9orf72 gene is the most common cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Several hypotheses have been proposed for how the mutation contributes to pathog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1064::ffbb7635de79d1bdd212f20803c16cfa
https://ora.ox.ac.uk/objects/uuid:b0e48523-2acc-4c1e-83a5-79696cbaf042
https://ora.ox.ac.uk/objects/uuid:b0e48523-2acc-4c1e-83a5-79696cbaf042
Autor:
Dafinca, R, Scaber, J, Ababneh, N, Lalic, T, Weir, G, Christian, H, Vowles, J, Douglas, AGL, Fletcher-Jones, A, Browne, C, Nakanishi, M, Turner, MR, Wade-Martins, R, Cowley, SA, Talbot, K
An expanded hexanucleotide repeat in a noncoding region of the C9orf72 gene is a major cause of amyotrophic lateral sclerosis (ALS), accounting for up to 40andpercnt; of familial cases and 7andpercnt; of sporadic ALS in European populations. We have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d416e5b68c0fbd02aa724deb92296115
https://eprints.soton.ac.uk/393755/
https://eprints.soton.ac.uk/393755/
Publikováno v:
In Journal of the Neurological Sciences 15 October 2015 357 Supplement 1:e48-e48
Autor:
Al-Ababneh, N.1 nedalk@just.edu.jo
Publikováno v:
International Journal of Electronics. Sep2007, Vol. 94 Issue 9, p845-855. 11p. 2 Diagrams, 5 Graphs.
Publikováno v:
24th IEEE International Conference on Advanced Information Networking & Applications (AINA), 2010; 2010, p600-606, 7p
Autor:
Ababneh, N., Labiod, H.
Publikováno v:
Ad Hoc Networking Workshop (Med-Hoc-Net), 2010 the 9th IFIP Annual Mediterranean; 2010, p1-8, 8p
Publikováno v:
2010 IEEE Sarnoff Symposium; 2010, p1-5, 5p
Publikováno v:
2009 IEEE International Symposium on a World of Wireless, Mobile & Multimedia Networks & Workshops; 2009, p1-9, 9p