DEFICIENCY OF LECITHIN, CHOLESTEROL ACYLTRANSFERASE DUE TO COMPOUND HETEROZYGOSITY OF 2 NOVEL MUTATIONS (GLY33ARG AND 30 BP INS) IN THE LCAT GENE

被引：0
|
作者：
WIEBUSCH, H
CULLEN, P
OWEN, JS
COLLINS, D
SHARP, PS
FUNKE, H
ASSMANN, G
机构：
[1] UNIV MUNSTER, INST ARTERIOSKLEROSEFORSCH, D-48149 MUNSTER, GERMANY
[2] UNIV LONDON, ROYAL FREE HOSP, SCH MED, DEPT MED, LONDON NW3 2PF, ENGLAND
[3] NORTHWICK PK HOSP & CLIN RES CTR, DEPT CLIN CHEM, HARROW HA1 3UJ, MIDDX, ENGLAND
[4] NORTHWICK PK HOSP & CLIN RES CTR, DEPT ENDOCRINOL, HARROW HA1 3UJ, MIDDX, ENGLAND
来源：
HUMAN MOLECULAR GENETICS | 1995年 / 4卷 / 01期
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：143 / 145
页数：3
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