Detalhe da pesquisa
1.
CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model.
Hum Mol Genet
; 24(16): 4584-98, 2015 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-25994508