WFRF:(Bindoff LA)
Search: WFRF:(Bindoff LA) > (2016) > A heterozygous 21-b...
- 1 of 1
- Previous record
- Next record
- To hitlist
A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy
- Vissing, J (author)
- Barresi, R (author)
- Witting, N (author)
- show more...
- Van Ghelue, M (author)
- Gammelgaard, L (author)
- Bindoff, LA (author)
- Straub, V (author)
- Lochmuller, H (author)
- Hudson, J (author)
- Wahl, CM (author)
- Dahlbom, K (author)
- Jonsrud, C (author)
- Duno, M (author)
- show less...
- (creator_code:org_t)
- 2016-06-03
- 2016
- English.
- In: Brain : a journal of neurology. - : Oxford University Press (OUP). - 1460-2156. ; 139:Pt 8, s. 2154-2163
- Journal article (peer-reviewed)
Subject headings
Close
Publication and Content Type
- ref (subject category)
- art (subject category)
Find in a library
- Brain : a journal of neurology (Search for host publication in LIBRIS)
To the university's database
- 1 of 1
- Previous record
- Next record
- To hitlist
Find more in SwePub
- By the author/editor
- Vissing, J
- Barresi, R
- Witting, N
- Van Ghelue, M
- Gammelgaard, L
- Bindoff, LA
- show more...
- Straub, V
- Lochmuller, H
- Hudson, J
- Wahl, CM
- Arnardottir, S
- Dahlbom, K
- Jonsrud, C
- Duno, M
- show less...
- Articles in the publication
- Brain : a journa ...
- Brain
- By the university
- Karolinska Institutet
Search outside SwePub
- Extend your search to:
- Google Book Search
- Google Scholar
Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.
- Copyright © LIBRIS - National Library Systems
- LIBRIS.kb.se
