Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity-Reference-Cited by-同舟云学术

Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity

Author:

Risinger Mary¹^ORCID,Christakopoulos Georgios E.²,Schultz Corinna L.³^ORCID,McGann Patrick T.⁴⁵,Zhang Wenying⁵⁶,Kalfa Theodosia A.⁴⁵^ORCID

Affiliation:

1. College of Nursing; University of Cincinnati; Cincinnati Ohio

2. Department of Pediatrics; University of Minnesota; Minneapolis; Minnesota

3. Nemours Center for Cancer and Blood Disorders; Nemours/Alfred I. duPont Hospital for Children; Wilmington Delaware

4. Cancer and Blood Diseases Institute; Cincinnati Children's Hospital Medical Center; Cincinnati Ohio

5. Department of Pediatrics; University of Cincinnati College of Medicine; Cincinnati Ohio

6. Laboratory of Genetics and Genomics; Division of Human Genetics; Cincinnati Children's Hospital Medical Center; Cincinnati Ohio

Funder

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

Reference22 articles.

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