SANFILIPPO-B DISEASE - SERUM ASSAYS FOR DETECTION OF HOMOZYGOUS AND HETEROZYGOUS INDIVIDUALS IN THREE FAMILIES

被引：30

作者：

FIGURA, KV ^{[1
]}

LOGERING, M ^{[1
]}

MERSMANN, G ^{[1
]}

KRESSE, H ^{[1
]}

机构：

[1] UNIV MUNSTER, INST PHYSIOL CHEM, WALDEYER STR 15, D44 MUNSTER, WEST GERMANY

来源：

JOURNAL OF PEDIATRICS | 1973年 / 83卷 / 04期

关键词：

D O I：

10.1016/S0022-3476(73)80222-7

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

收藏

页码：607 / 611

页数：5

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[4] MCKUSICK VA, 1966, HERITABLE DISORDERS
[5] SANFILIPPO SYNDROME - PROFOUND DEFICIENCY OF ALPHA-ACETYLGLUCOSAMINIDASE ACTIVITY IN ORGANS AND SKIN FIBROBLASTS FROM TYPE-B PATIENTS
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1972, 69 (07) : 1720 - &
[6] REISSIG L, 1955, J BIOL CHEM, V217, P959
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