Skip to main content

CORRECTION article

Front. Physiol., 18 October 2019
Sec. Red Blood Cell Physiology
Volume 10 - 2019 | https://doi.org/10.3389/fphys.2019.01331
This article is part of the Research Topic Pathophysiology of Rare Hemolytic Anemias View all 15 articles

Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis

This article is a correction to:

  1. The Spectrum of SPTA1-Associated Hereditary Spherocytosis

    1. Read original article
\nSatheesh Chonat,Satheesh Chonat1,2Mary RisingerMary Risinger3Haripriya SakthivelHaripriya Sakthivel4Omar Niss,Omar Niss4,5Jennifer A. RothmanJennifer A. Rothman6Loan HsiehLoan Hsieh7Stella T. Chou,Stella T. Chou8,9Janet L. Kwiatkowski,Janet L. Kwiatkowski8,9Eugene Khandros,Eugene Khandros8,9Matthew F. GormanMatthew F. Gorman10Donald T. WellsDonald T. Wells11Tamara MaghatheTamara Maghathe4Neha DagaonkarNeha Dagaonkar12Katie G. SeuKatie G. Seu4Kejian ZhangKejian Zhang13Wenying Zhang,Wenying Zhang5,14Theodosia A. Kalfa, Theodosia A. Kalfa4,5*
  • 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.

TABLE 1
www.frontiersin.org

Table 1. Genetic mutations and associated phenotype in HS due to SPTA1 mutations.

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.

References

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

PubMed Abstract | CrossRef Full Text | Google Scholar

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, dGhlb2Rvc2lhLmthbGZhJiN4MDAwNDA7Y2NobWMub3Jn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.