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Leukemia & Lymphoma Volume 60, 2019 - Issue 13
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Letters to the Editor

Phenotypic heterogeneity associated with germline GATA2 haploinsufficiency: a comprehensive kindred study

Candace L. HaddoxDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA; ORCID Iconhttp://orcid.org/0000-0003-4223-0632
ORCID Icon,
Ryan M. CarrDivision of Hematology, Mayo Clinic, Rochester, MN, USA;
,
Roshini S. AbrahamDepartment of Pathology and Laboratory Medicine, Nationwide Children’s Hospital, Columbus, OH, USA; ;Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA;
,
Juliana Perez BoteroDivision of Hematology, Mayo Clinic, Rochester, MN, USA;
,
Vilmarie RodriguezDivision of Pediatric Hematology and Oncology, Mayo Clinic, Rochester, MN, USA
,
Animesh PardananiDivision of Hematology, Mayo Clinic, Rochester, MN, USA;
&
Mrinal M. PatnaikDivision of Hematology, Mayo Clinic, Rochester, MN, USA; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0001-6998-662X
ORCID Icon show all
Pages 3282-3286 | Received 25 May 2018, Accepted 11 Jun 2019, Published online: 27 Jun 2019
 
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Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at https://doi.org/10.1080/10428194.2019.1633630.

Acknowledgments

Current publication is supported in part by grants from the ‘The Gerstner Family Career Development Award’ and the ‘Mayo Clinic Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA’. This publication was supported by CTSA Grant Number KL2 TR000136 from the National Center for Advancing Translational Science (NCATS). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.

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