Detalhe da pesquisa
1.
A novel missense mutation in the MYH7 gene causes an uncharacteristic phenotype of myosin storage myopathy: a case report.
BMC Med Genet
; 20(1): 78, 2019 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31068177
2.
Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6.
Hum Mol Genet
; 25(18): 4062-4079, 2016 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27466185
3.
Adenovirus serotype 14 infection, New Brunswick, Canada, 2011.
Emerg Infect Dis
; 19(1): 119-22, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23260201