Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis
- 1Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, United States
- 2Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA, United States
- 3College of Nursing, University of Cincinnati, Cincinnati, OH, United States
- 4Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
- 5Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States
- 6Duke University Medical Center, Durham, NC, United States
- 7Division of Hematology, CHOC Children's Hospital and UC Irvine Medical Center, Orange, CA, United States
- 8Division of Hematology, Children's Hospital of Philadelphia, Philadelphia, PA, United States
- 9Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States
- 10Kaiser Permanente Santa Clara Medical Center, Santa Clara, CA, United States
- 11Dell Children's Medical Center, Austin, TX, United States
- 12Genomics Analysis Facility, Institute for Genomic Medicine, Columbia University, New York, NY, United States
- 13Coyote Bioscience Co., Ltd., San Jose, CA, United States
- 14Laboratory of Genetics and Genomics, Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
A Corrigendum on
The Spectrum of SPTA1-Associated Hereditary Spherocytosis
by Chonat, S., Risinger, M., Sakthivel, H., Niss, O., Rothman, J. A., Hsieh, L., et al. (2019). Front. Physiol. 10:815. doi: 10.3389/fphys.2019.00815
In the original article, there was a mistake in Table 1 as published. The SPTA1 mutation of Allele 2 in Patient 1, is stated as “c.4294T>A (p.L1432*).” The correct mutation should read “c.4295del (p.L1432*).” The corrected Table 1 appears below.
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Bogardus, H., Schulz, V. P., Maksimova, Y., Miller, B. A., Li, P., Forget, B. G., et al. (2014). Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus. Haematologica 99, e168–e170. doi: 10.3324/haematol.2014.110312
Keywords: SPTA1, α-spectrin, αLEPRA, hereditary spherocytosis, next generation sequencing, hemolytic anemia, hydrops fetalis
Citation: Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W and Kalfa TA (2019) Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis. Front. Physiol. 10:1331. doi: 10.3389/fphys.2019.01331
Received: 03 September 2019; Accepted: 04 October 2019;
Published: 18 October 2019.
Edited by:Paola Bianchi, IRCCS Ca 'Granda Foundation Maggiore Policlinico Hospital, Italy
Reviewed by:Elisa Fermo, IRCCS Ca 'Granda Foundation Maggiore Policlinico Hospital, Italy
Copyright © 2019 Chonat, Risinger, Sakthivel, Niss, Rothman, Hsieh, Chou, Kwiatkowski, Khandros, Gorman, Wells, Maghathe, Dagaonkar, Seu, Zhang, Zhang and Kalfa. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Theodosia A. Kalfa, firstname.lastname@example.org