Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patient.

Human mutation

Volumn 16, Issue 4, 2000, Pages 374-

  Gutierrez, G ^a   Schneider, A ^a   Jobs, J ^a   Schmidt, H ^a   Korte, A ^a   Manns, M P ^a   Stuhrmann, M ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; TRYPTOPHAN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; FEMALE; GENETICS; HOMOZYGOTE; HUMAN; HYPERLIPOPROTEINEMIA TYPE 2; POINT MUTATION; PRESCHOOL CHILD; TURKEY (REPUBLIC);

ADULT; AMINO ACID SUBSTITUTION; ARGININE; CHILD, PRESCHOOL; FEMALE; HOMOZYGOTE; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; POINT MUTATION; TRYPTOPHAN; TURKEY;

EID: 0034292838     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200010)16:4<374::AID-HUMU16>3.0.CO;2-1     Document Type: Article

References (0)