LESCH-NYHAN SYNDROME - MOLECULAR INVESTIGATION OF 3 FRENCH-CANADIAN FAMILIES USING A HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE CDNA PROBE

被引：18

作者：

SINNETT, D ^{[1
]}

LAVERGNE, L ^{[1
]}

MELANCON, SB ^{[1
]}

DALLAIRE, L ^{[1
]}

POTIER, M ^{[1
]}

LABUDA, D ^{[1
]}

机构：

[1] UNIV MONTREAL,HOP ST JUSTINE,CTR RECH PEDIAT,MONTREAL H3T 1C5,QUEBEC,CANADA

来源：

HUMAN GENETICS | 1988年 / 81卷 / 01期

关键词：

D O I：

10.1007/BF00283719

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：4 / 8

页数：5

共 35 条

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[12]

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[13]

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[18]

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[19] ADENINE PHOSPHORIBOSYL TRANSFERASE DEFICIENCY IN ASSOCIATION WITH SUB-NORMAL HYPOXANTHINE PHOSPHORIBOSYL TRANSFERASE IN FAMILIES OF LESCH-NYHAN PATIENTS [J].

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[20] ISOLATION AND CHARACTERIZATION OF A FULL-LENGTH EXPRESSIBLE CDNA FOR HUMAN HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE [J].

JOLLY, DJ ;

OKAYAMA, H ;

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