Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations

American Journal of Human Genetics

Volumn 48, Issue 3, 1991, Pages 546-551

  Kang, S S ^a   Wong, P W K ^a   Bock, H G O ^a   Horwitz, A ^a   Grix, A ^a  

^a RUSH UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE;

ARTICLE; BLOOD LEVEL; CASE REPORT; ENZYME DEFICIENCY; HETEROZYGOSITY; HUMAN; MUTANT; PEDIGREE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; ALLELES; AMINE OXIDOREDUCTASES; AMINO ACID METABOLISM, INBORN ERRORS; ENZYME ACTIVATION; FEMALE; FOLIC ACID; HEAT; HETEROZYGOTE; HOMOCYSTEINE; HUMAN; INFANT, NEWBORN; LYMPHOCYTES; MALE; MUTATION; PEDIGREE; SUBSTRATE SPECIFICITY; SUPPORT, U.S. GOV'T, P.H.S.; VITAMIN B 12;

EID: 0026088764     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)