A Japanese patient with lipoprotein lipase deficiency homozygous for the Gly188Glu mutation prevalent worldwide.

Journal of atherosclerosis and thrombosis

Volumn 7, Issue 1, 2000, Pages 45-49

  Yoshida, T ^a   Gotoda, T ^a   Okubo, M ^a   Iizuka, Y ^a   Ishibashi, S ^a   Kojima, T ^a   Murakami, T ^a   Murase, T ^a   Yamada, N ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

LIPOPROTEIN LIPASE;

ADULT; ARTICLE; BLOOD; CASE REPORT; CHILD; FEMALE; GENETICS; HAPLOTYPE; HOMOZYGOTE; HUMAN; HYPERLIPOPROTEINEMIA TYPE 1; INFANT; JAPAN; MALE; PEDIGREE; POINT MUTATION; PRESCHOOL CHILD; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; HAPLOTYPES; HOMOZYGOTE; HUMANS; HYPERLIPOPROTEINEMIA TYPE I; INFANT; JAPAN; LIPOPROTEIN LIPASE; MALE; PEDIGREE; POINT MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0034577331     PISSN: 13403478     EISSN: None     Source Type: Journal    
DOI: 10.5551/jat1994.7.45     Document Type: Article

References (0)