Detalhe da pesquisa
1.
Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.
Hum Mol Genet
; 28(14): 2378-2394, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31090908
2.
A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.
J Neuromuscul Dis
; 9(1): 193-210, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34602496
3.
Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H.
Am J Hum Genet
; 81(1): 1-16, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17564959