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Blood Cells Mol Dis. 2020 Jan 10;81:102390. doi: 10.1016/j.bcmd.2019.102390. [Epub ahead of print]

Corrigendum to "Combined genetic disruption of K-Cl cotransporters and Gardos channel KCNN4 rescues erythrocyte dehydration in the SAD mouse model of sickle cell disease" [Blood Cells Mol. Dis. (2019) start page-end page not yet assigned] https://doi.org/10.1016/j.bcmd.2019.102346.

Author information

1
Renal Division and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, MA, United States of America; Department of Laboratory Medicine, Boston Children's Hospital, Boston, MA 02115, United States of America.
2
Renal Division and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, MA, United States of America; Department of Medicine, Harvard Medical School, Boston, MA 02115, United States of America; Department of Pathology, Harvard Medical School, Boston, MA 02115, United States of America.
3
Department of Laboratory Medicine, UCSF, San Francisco, CA, United States of America.
4
Renal Division and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, MA, United States of America.
5
Institut de Recherches Cliniques de Montreal, Molecular Genetics and Development, Faculte de Medecine, Universite of Montreal, Montreal, Quebec, Canada.
6
Institute of Physiological Chemistry, Philipps-Universit├Ąt Marburg, Marburg, Germany.
7
Institute of Human Genetics, Universitatsklinikum Jena, Jena, Germany.
8
Department of Laboratory Medicine, Boston Children's Hospital, Boston, MA 02115, United States of America; Department of Pathology, Harvard Medical School, Boston, MA 02115, United States of America.
9
Renal Division and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Boston, MA, United States of America; Department of Medicine, Harvard Medical School, Boston, MA 02115, United States of America. Electronic address: salper@bidmc.harvard.edu.
PMID:
31931456
DOI:
10.1016/j.bcmd.2019.102390

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