Detalhe da pesquisa
1.
The role of de novo mutations in the development of amyotrophic lateral sclerosis.
Hum Mutat
; 38(11): 1534-1541, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28714244
2.
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
Hum Mol Genet
; 23(8): 2220-31, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24256812
3.
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy.
Neurobiol Aging
; 35(8): 1956.e9-1956.e11, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24612671