ROCKEFELLER UNIVERSITY
Genetic basis of incomplete penetrance of RPSA haploinsufficiency for congenital asplenia
Genetic basis of incomplete penetrance of RPSA haploinsufficiency for congenital asplenia is a funding opportunity from ROCKEFELLER UNIVERSITY, up to 466125, closing June 30, 2027.
Jun 30, 2027
(334d left)Overview
PROJECT SUMMARY Isolated congenital asplenia (ICA) is characterized by the absence of a spleen at birth without any detectable associated developmental abnormalities (OMIM #271400). ICA is the only known human developmental defect affecting only a lymphoid organ. Patients with ICA are prone to life-threatening…