Two Different Allelic Mutations in a Finnish Family With...

Two Different Allelic Mutations in a Finnish Family With Lecithin:Cholesterol Acyltransferase Deficiency

Miettinen, H., Gylling, H., Ulmanen, I., Miettinen, T. A., Kontula, K.
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Volume:
15
Language:
english
Journal:
Arteriosclerosis, Thrombosis, and Vascular Biology
DOI:
10.1161/01.atv.15.4.460
Date:
April, 1995
File:
PDF, 1.26 MB
english, 1995
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