Human congenital hypotransferrinemia is a rare disorder characterized by the virtual absence of transferrin in the serum. No information on the causes of the disease is known.

Goldwurm, S., Casati, C., Venturi, N., Strada, S., Santambrogio, P., Indraccolo, S., et al. (2000). Biochemical and genetic defects underlying human congenital hypotransferrinemia. HEMATOLOGY JOURNAL, 1(6), 390-398 [10.1038/sj/thj/6200063].

Biochemical and genetic defects underlying human congenital hypotransferrinemia

PIPERNO, ALBERTO;MASERA, GIUSEPPE;BIONDI, ANDREA
2000

Abstract

Human congenital hypotransferrinemia is a rare disorder characterized by the virtual absence of transferrin in the serum. No information on the causes of the disease is known.
Articolo in rivista - Articolo scientifico
Atransferrinemia; Histocompatibility Antigens Class I; Humans; Infant, Newborn; Liver; Transferrin; Membrane Proteins;
English
390
398
9
Goldwurm, S., Casati, C., Venturi, N., Strada, S., Santambrogio, P., Indraccolo, S., et al. (2000). Biochemical and genetic defects underlying human congenital hypotransferrinemia. HEMATOLOGY JOURNAL, 1(6), 390-398 [10.1038/sj/thj/6200063].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/58249
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