A mutation (T-45C) in the promoter region of the low-density-lipoprotein (LDL)-receptor gene is associated with a mild clinical phenotype in a patient with heterozygous familial hypercholesterolaemia (FH)
Sun, X.-M., Neuwirth, C., Wade, D. P., Knight, B. L., Soutar, A. K.Volume:
4
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/4.11.2125
Date:
November, 1995
File:
PDF, 4.92 MB
english, 1995