Alina Kurolap
0000-0002-7005-3621
2 papers found
Refreshing results…
Pathogenic variants in SMARCA5 , a chromatin remodeler, cause a range of syndromic neurodevelopmental features
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis
Missing publications? Search for publications with a matching author name.