Associated Papers
Global analysis of suppressor mutations that rescue human genetic defects.
Ünlü B et al.
Genome Medicine, 2023
37821946 (PubMed )
Supplement: 13073_2023_1232_MOESM3_ESM.xlsx › Data
Growth factor and receptor malfunctions associated with human genetic deafness.
Naz S et al.
Clinical Genetics, 2020
Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.
Yousaf R et al.
The Journal of Clinical Investigation, 2018
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