A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype
Author:
Affiliation:
1. Department of Human Pathology of Adult and Developmental Age ‘Gaetano Barresi’, ‘Gaetano Martino’ University Hospital of Messina, Messina, Italy
Publisher
Informa UK Limited
Subject
Hematology,Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10245332.2017.1317990
Reference23 articles.
1. Malabsorption and defective utilization of iron in three siblings
2. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)
3. Matriptase-2, a Membrane-bound Mosaic Serine Proteinase Predominantly Expressed in Human Liver and Showing Degrading Activity against Extracellular Matrix Proteins
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