Human transferrin (Tf): A single mutation at codon 570 determines Tf C1 or Tf C2 variant

Human Genetics

Volumn 100, Issue 3-4, 1997, Pages 457-458

  Namekata, Kazuhiko ^a   Oyama, Fumitaka ^a   Imagawa, Masaki ^b   Ihara, Yasuo ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b HYOGO PREFECTURAL AMAGASAKI GENERAL MEDICAL CENTER   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFERRIN;

AMINO ACID SUBSTITUTION; ARTICLE; EXON; GENOTYPE; HUMAN; HUMAN CELL; ISOELECTRIC FOCUSING; NUCLEIC ACID BASE SUBSTITUTION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN POLYMORPHISM;

CODON; GENOTYPE; HUMANS; MUTATION; POLYMERASE CHAIN REACTION; TRANSFERRIN;

EID: 0030923505     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050533     Document Type: Article

References (3)

1. Kamboh MI, Ferrell RE (1987) Human transferrin polymorphism. Hum Hered 37:65-81
2. Rensburg SJ Van, Carstens ME, Potocnik FC, Aucamp AK, Taljaard JF (1993) Increased frequency of the transferrin C2 sub-type in Alzheimer's disease. Neuroreport 4:1269-1271
3. Yang F, Lum JB, McGill JR, Moore CM, Naylor SL, Bragt PH Van, Baldwin WD, Bowman BH (1984) Human transferrin: cDNA characterization and chromosomal localization. Proc Natl Acad Sci USA 81:2752-2756