Detalhe da pesquisa
1.
Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene.
BMC Med Genomics
; 15(1): 78, 2022 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379233
2.
Identification of hub genes associated with RNAi-induced silencing of XIAP through targeted proteomics approach in MCF7 cells.
Cell Biosci
; 10: 78, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32537125