MOLECULAR-BASIS OF THE COMMON ELECTROPHORETIC POLYMORPHISM (FU1/FU2) IN HUMAN ALPHA-L-FUCOSIDASE

被引：5

作者：

CRAGG, H

WINCHESTER, B

SEO, HC

OBRIEN, J

SWALLOW, D

机构：

[1] UNIV CALIF SAN DIEGO,DEPT NEUROSCI,LA JOLLA,CA 92093

[2] UNIV CALIF SAN DIEGO,CTR MOLEC GENET,LA JOLLA,CA 92093

[3] UNIV LONDON UNIV COLL,GALTON LAB,MRC,HUMAN BIOCHEM GENET UNIT,LONDON NW1 2HE,ENGLAND

来源：

JOURNAL OF MEDICAL GENETICS | 1994年 / 31卷 / 08期

关键词：

D O I：

10.1136/jmg.31.8.659-a

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：659 / 660

页数：2

共 15 条

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[12]

TURNER BM, 1975, AM J HUM GENET, V27, P651

[13]

WILLEMS P, 1990, THESIS U ANTWERP

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OBRIEN, JS .

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[15] A 5' SPLICE SITE MUTATION IN FUCOSIDOSIS [J].

WILLIAMSON, M ;

CRAGG, H ;

GRANT, J ;

KRETZ, K ;

OBRIEN, J ;

WILLEMS, PJ ;

YOUNG, E ;

WINCHESTER, B .

JOURNAL OF MEDICAL GENETICS, 1993, 30 (03) :218-223

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