Exploring Antisense Oligonucleotides as a potential therapy for Autosomal Dominant Leukodystrophy

$373,796R33FY2021NSNIH

University Of Pittsburgh At Pittsburgh, Pittsburgh PA

Investigators

Quasar S Padiathcontact

Linked publications & trials

Paper 37542275 Paper 35953447 Paper 35488860 Paper 32463361 Paper 32187401

View original record on NIH RePORTER →

Exploring Antisense Oligonucleotides as a potential therapy for Autosomal Dominant Leukodystrophy · GrantIndex