Detalhe da pesquisa
1.
Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder.
Brain
; 144(10): e85, 2021 11 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34373908
2.
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.
Genes (Basel)
; 12(11)2021 11 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34828389
3.
Tuberous Sclerosis Complex: Clinical Spectrum and Epilepsy: A Retrospective Chart Review Study.
Transl Neurosci
; 9: 154-160, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30479846