Profiles

Keywords
Last Name
Institution

Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects.

Bhatt N, Loew JM, Gallagher P, Mittal N. Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects. Pediatr Blood Cancer. 2019 01; 66(1):e27480.

View in: PubMed

collapse authors with profiles