Detalhe da pesquisa
1.
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Neurogenetics
; 24(4): 279-289, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37597066
2.
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Neurogenetics
; 24(4): 317-318, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37668767
3.
Exploring TTN variants as genetic insights into cardiomyopathy pathogenesis and potential emerging clues to molecular mechanisms in cardiomyopathies.
Sci Rep
; 14(1): 5313, 2024 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38438525
4.
Chromosome 9 Inversion: Pathogenic or Benign? A Comprehensive Systematic Review of all Clinical Reports.
Curr Mol Med
; 22(5): 385-400, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34365947
5.
Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia.
Front Genet
; 12: 625959, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33732287