Detalhe da pesquisa
1.
Guidelines for investigating causality of sequence variants in human disease.
Nature
; 508(7497): 469-76, 2014 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-24759409
2.
Exploring the relationship between α-actinin-3 deficiency and obesity in mice and humans.
Int J Obes (Lond)
; 41(7): 1154-1157, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28293018
3.
Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'.
Mol Psychiatry
; 19(8): 859-61, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24145379
4.
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy.
Neuromuscul Disord
; 27(11): 1043-1046, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28803818
5.
Corrigendum to "A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy" [Neuromuscular disorders 27/11 (2017) 1043-1046].
Neuromuscul Disord
; 28(1): 101, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29246662
6.
A gene for speed: contractile properties of isolated whole EDL muscle from an alpha-actinin-3 knockout mouse.
Am J Physiol Cell Physiol
; 295(4): C897-904, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18650267