Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism.
作者信息
Berg K, Heiberg A
出版信息
Cytogenet Cell Genet. 1976;16(1-5):266-70. doi: 10.1159/000130606.
PMID:975887
Abstract
摘要
相似文献
1
Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism.
Cytogenet Cell Genet. 1976;16(1-5):266-70. doi: 10.1159/000130606.
2
Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism.
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Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed.
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Probable linkage between essential familial hypercholesterolemia and third complement component (C3).
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Probable linkage between essential familial hypercholesterolemia and third complement component (C3).
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The inheritance of hyperlipoproteinaemia with xanthomatosis. A study of 132 kindreds.伴有黄瘤病的高脂蛋白血症的遗传。对132个家族的研究。
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Acta Clin Belg. 1969;24(5):276-86. doi: 10.1080/17843286.1969.11716722.
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Essential familial hypercholesterolemia with xanthomatosis.伴有黄瘤病的家族性高胆固醇血症
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[Fredrickson type II hyperlipoproteinemia].
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The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19.载脂蛋白E（apoE）基因座位于19号染色体上，靠近路德（Lu）血型基因座。
Hum Genet. 1984;67(2):178-82. doi: 10.1007/BF00272996.
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