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Publikováno v:
Journal of human genetics. 47(7)
We previously reported a patient with hereditary hypotransferrinemia who suffered from severe anemia and growth retardation and was diagnosed on the basis of an extremely low level of serum transferrin (TF). By an isoelectric focusing analysis, we fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::238f60cc30983c636cfce6fd7b9a2559
https://pubmed.ncbi.nlm.nih.gov/12111369
https://pubmed.ncbi.nlm.nih.gov/12111369
