Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rheenen, W. van"'
Autor:
Diekstra, F.P., Vught, P.W. van, Rheenen, W. van, Koppers, M., Pasterkamp, R.J., Es, M.A. van, Schelhaas, H.J., Visser, M. de, Robberecht, W., Damme, P. van, Andersen, P.M., Berg, L.H. van den, Veldink, J.H.
Publikováno v:
Neurobiology of Aging, 33, 630.e3-8
Neurobiology of Aging, 33, 3, pp. 630.e3-8
Neurobiology of Aging, 33, 3, pp. 630.e3-8
Item does not contain fulltext A large genome-wide screen in patients with sporadic amyotrophic lateral sclerosis (ALS) showed that the common variant rs12608932 in gene UNC13A was associated with disease susceptibility. UNC13A regulates the release
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::dfb879bd80f5c36aa2d661574c838cf5
http://hdl.handle.net/2066/110085
http://hdl.handle.net/2066/110085
Autor:
Doormaal, P.T. van, Rheenen, W. van, Blitterswijk, M. van, Schellevis, R.D., Schelhaas, H.J., Visser, M. de, Kooi, A.J. van der, Veldink, J.H., Berg, L.H. van den
Publikováno v:
Neurobiology of Aging, 33, 9, pp. 2233.e7-2233.e8
Neurobiology of Aging, 33, 2233.e7-2233.e8
Neurobiology of Aging, 33, 2233.e7-2233.e8
Item does not contain fulltext Recently it was discovered that mutations in the UBQLN2 gene were a cause of an X-linked dominant type of familial amyotrophic lateral sclerosis (ALS). We investigated the frequency of mutations in this gene in a cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e8ad91c3453a3781b53524ee1ca0e9ad
https://hdl.handle.net/2066/110084
https://hdl.handle.net/2066/110084