Associated Papers
Structural Insights into the Mechanisms Underlying Polyaminopathies.
Wu B et al.
International Journal of Molecular Sciences, 2024
Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorder.
Alayoubi AM et al.
Scientific Reports, 2024
A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage.
Liang M et al.
Molecular Genetics & Genomic Medicine, 2024
38400599 (PubMed )
Supplement: MGG3-12-e2402-s001.pdf
Integrative analysis of mutational and transcriptional profiles reveals driver mutations of metastatic breast cancers.
Lee JH et al.
Cell Discovery, 2016
27625789 (PubMed )
Supplement: celldisc201625-s8.pdf
Select a paper to view details