Compound heterozygosity in PKLR gene for a previously unrecognized intronic polymorphism and a rare missense mutation as a novel cause of severe pyruvate kinase deficiency
Shruti Bagla,
Kanta Bhambhani,
Manisha Gadgeel,
Steven Buck,
Jian-Ping Jin,
Yaddanapudi Ravindranath
Affiliations
Shruti Bagla
Division of Hematology/Oncology, Department of Pediatrics, Wayne State University – School of Medicine, and Children’s Hospital of Michigan
Kanta Bhambhani
Division of Hematology/Oncology, Department of Pediatrics, Wayne State University – School of Medicine, and Children’s Hospital of Michigan
Manisha Gadgeel
Division of Hematology/Oncology, Department of Pediatrics, Wayne State University – School of Medicine, and Children’s Hospital of Michigan
Steven Buck
Division of Hematology/Oncology, Department of Pediatrics, Wayne State University – School of Medicine, and Children’s Hospital of Michigan
Jian-Ping Jin
Department of Physiology, Wayne State University, School of Medicine, Detroit, MI, USA
Yaddanapudi Ravindranath
Division of Hematology/Oncology, Department of Pediatrics, Wayne State University – School of Medicine, and Children’s Hospital of Michigan