COMPLETE DEFICIENCY OF PLASMA LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) ACTIVITY DUE TO A NOVEL HOMOZYGOUS MUTATION (GLY-30-SER) IN THE LCAT GENE

Authors
OWEN JS WIEBUSCH H CULLEN P WATTS GF LIMA VLM FUNKE H ASSMANN G
Citation
Js. Owen et al., COMPLETE DEFICIENCY OF PLASMA LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) ACTIVITY DUE TO A NOVEL HOMOZYGOUS MUTATION (GLY-30-SER) IN THE LCAT GENE, Human mutation, 8(1), 1996, pp. 79-82
Citations number
15
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
8
Issue
1
Year of publication
1996
Pages
79 - 82
Database
ISI
SICI code
1059-7794(1996)8:1<79:CDOPLA>2.0.ZU;2-Q