The transcobalamin codon 259 polymorphism should be designated 776C>G, not 775G>C [2] (multiple letters)

Blood

Volumn 101, Issue 9, 2003, Pages 3749-3751

  Zetterberg, Henrik ^a   Palmér, Mona ^c   Boreström, Cecilia ^c   Rymo, Lars ^c   Blennow, Kaj ^c   Miller, Joshua W ^b   Green, Ralph ^c  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYANOCOBALAMIN; PROLINE; TRANSCOBALAMIN; ENDODEOXYRIBONUCLEASE BSTNI; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

AMINO ACID SUBSTITUTION; CODON; CYANOCOBALAMIN DEFICIENCY; DNA SEQUENCE; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LETTER; NUCLEOTIDE SEQUENCE; PHENOTYPIC VARIATION; PRIORITY JOURNAL; ADULT; AGED; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; NOMENCLATURE; NOTE; POLYMERASE CHAIN REACTION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADULT; AGED; ARGININE; CODON; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MIDDLE AGED; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PROLINE; TERMINOLOGY; TRANSCOBALAMINS; VITAMIN B 12 DEFICIENCY;

EID: 0038204135     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2003-01-0135     Document Type: Letter

References (0)