CARRIER DETECTION IN ORNITHINE TRANSCARBAMYLASE DEFICIENCY

被引：21

作者：

HAAN, EA

DANKS, DM

GRIMES, A

HOOGENRAAD, NJ

机构：

[1] UNIV MELBOURNE,ROYAL CHILDRENS HOSP,DEPT PEDIAT,GENET RES UNIT,PARKVILLE,VIC 3052,AUSTRALIA

[2] LA TROBE UNIV,DEPT BIOCHEM,BUNDOORA,VIC 3083,AUSTRALIA

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1982年 / 5卷 / 01期

关键词：

D O I：

10.1007/BF01799752

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：37 / 40

页数：4

共 18 条

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[3]

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[7] CARRIER DETECTION IN ORNITHINE TRANSCARBAMYLASE DEFICIENCY [J].

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IDEMOTO, J ;

SCHAFER, IA .

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[8]

HSIA YE, 1974, GASTROENTEROLOGY, V67, P347

[9] HYPERAMMONAEMIA - A VARIANT TYPE OF DEFICIENCY OF LIVER ORNITHINE TRANSCARBAMYLASE [J].

LEVIN, B ;

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[10]

LEVIN B, 1969, LANCET, V2, P170

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