INHERITANCE OF ENZYME DEFICIENCY IN 3 NEUROLIPIDOSES - VARIANT-O OF TAY-SACHS DISEASE (SANDHOFFS DISEASE), CLASSIC TAY-SACHS DISEASE, AND METACHROMATIC LEUKODYSTROPHY - IDENTIFICATION OF HETEROZYGOUS CARRIERS

被引：16

作者：

HARZER, K ^{[1
]}

机构：

[1] UNIV TUBINGEN,INST HIRN FORSCH,KORBINIAN BRODMANN HAUS,BELTHLE STR 15,7400 TUBINGEN,WEST GERMANY

来源：

HUMANGENETIK | 1973年 / 20卷 / 01期

关键词：

D O I：

10.1007/BF00280871

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：9 / 24

页数：16

相关论文

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