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Paper Details

Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation.
J Exp Med
26
2019
C, GATA1, alternative splice acceptor site, amino acid, canonical splice acceptor site, dyserythropoietic anemia, genetic blood disorders, human, impairments in hematopoiesis, noncoding variants, patients, zinc
Author NameAffiliation
Jacob C UlirschThe Manton Center for Orphan Disease Research, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School
Jacob C UlirschHarvard Medical School
Jacob C UlirschBroad Institute of MIT and Harvard
Namrata GuptaBroad Institute of MIT and Harvard
Stacey GabrielBroad Institute of MIT and Harvard
Stacey GabrielBroad Institute of MIT and Harvard
Benjamin L EbertBroad Institute of MIT and Harvard
Benjamin L EbertBrigham and Women's Hospital
Benjamin L EbertDana-Farber Cancer Institute
Charlotte M NiemeyerMedical Center-University of Freiburg
Charlotte M Niemeyer
Charlotte M NiemeyerGerman Cancer Research Center
Vijay G SankaranThe Manton Center for Orphan Disease Research, Boston Children's Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School
Vijay G SankaranBroad Institute of MIT and Harvard
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