Nicoletta Resta
0000-0001-8640-5532
4 papers found
Refreshing results…
Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Functional evidence of mTORβ splice variant involvement in the pathogenesis of congenital heart defects
Old treatments for new genetic conditions: Sirolimus therapy in a child affected by mosaic overgrowth with fibroadipose hyperplasia
Missing publications? Search for publications with a matching author name.