Detalhe da pesquisa
1.
Correction to: Novel mutations in KMT2B offer pathophysiological insights on childhood-onset progressive dystonia.
J Hum Genet;
64(10): 1051-1054, 2019 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31388109
2.
Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia.
J Hum Genet;
64(8): 803-813, 2019 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31165786
3.
Deep brain stimulation in rapidly progressive Parkinson-dystonia syndrome due to mitochondrial disorder.
Parkinsonism Relat Disord;
18(5): 672-4, 2012 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22104013