Gábor Mátyás
0000-0002-3212-9963
Foundation for People with Rare Diseases
3 papers found
Refreshing results…
Potential of whole-genome sequencing-based pharmacogenetic profiling
Variant filtering, digenic variants, and other challenges in clinical sequencing: a lesson from fibrillinopathies
Celiprolol but not losartan improves the biomechanical integrity of the aorta in a mouse model of vascular Ehlers–Danlos syndrome
Missing publications? Search for publications with a matching author name.