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Biochemical and genetic defects underlying human congenital hypotransferrinemia

Biochemical and genetic defects underlying human congenital hypotransferrinemia

Authors :
Goldwurm, S
Casati, C
Venturi, N
Strada, S
Santambrogio, P
Indraccolo, S
Arosio, P
Cazzola, M
Piperno, A
Masera, G
Biondi, A
PIPERNO, ALBERTO
MASERA, GIUSEPPE
BIONDI, ANDREA
Goldwurm, S
Casati, C
Venturi, N
Strada, S
Santambrogio, P
Indraccolo, S
Arosio, P
Cazzola, M
Piperno, A
Masera, G
Biondi, A
PIPERNO, ALBERTO
MASERA, GIUSEPPE
BIONDI, ANDREA
Publication Year :
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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1308912580
Document Type :
Electronic Resource