檢索結果 - Ansorge, Olaf
- Showing 1 - 20 results of 76
- Go to Next Page
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
-
10
-
11
-
12
-
13
-
14
-
15
-
16
-
17
-
18
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion() 由 Waite, Adrian J., Bäumer, Dirk, East, Simon, Neal, James, Morris, Huw R., Ansorge, Olaf, Blake, Derek J.
出版 2014Text -
19
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP 由 Nolan, Matthew, Barbagallo, Paola, Turner, Martin R, Keogh, Michael John, Chinnery, Patrick F, Talbot, Kevin, Ansorge, Olaf
出版 2021Text -
20