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Homozygous familial hypercholesterolemia: A novel point mutation (W556R) in a Turkish patient
Author(s) -
Gutierrez Gertha,
Schneider Andrea,
Jobs Jared,
Schmidt Hartmut,
Korte Andrea,
Manns Michael P.,
Stuhrmann Manfred
Publication year - 2000
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/1098-1004(200010)16:4<374::aid-humu16>3.0.co;2-1
Subject(s) - hepatology , medicine , medical school , gastroenterology , family medicine , medical education