HYPERPROLINEMIA TYPE-II

被引：20

作者：

APPLEGARTH, DA ^{[1
]}

INGRAM, P ^{[1
]}

HINGSTON, J ^{[1
]}

HARDWICK, DF ^{[1
]}

机构：

[1] UNIV BRITISH COLUMBIA, DEPT PAEDIAT, 715 W 12TH AVE, VANCOUVER 9, BRITISH COLUMBI, CANADA

来源：

关键词：

D O I：

10.1016/S0009-9120(74)90174-X

中图分类号：

R446 [实验室诊断]; R-33 [实验医学、医学实验];

学科分类号：

1001 ;

摘要：

引用

页码：14 / 28

页数：15

共 18 条

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[4] FAMILIAL HYPERPROLINEMIA - REPORT OF A 2ND CASE ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION WITH DEMONSTRATION OF AN ENZYME DEFECT
EFRON, ML
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1965, 272 (24) : 1243 - +
[5] Emery F A, 1968, J Ment Defic Res, V12, P187
[6] IRVINE DG, 1973, INT REV NEUROBIOL, V16, P112
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[8] JOHNSON A, 1965, J BIOL CHEM, V237, P1876
[9] PERRY TL, 1966, CAN MED ASSOC J, V95, P89
[10] HYPERPROLINAEMIA IN 2 SUCCESSIVE GENERATIONS OF A NORTH AMERICAN INDIAN FAMILY
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HARDWICK, DF
LOWRY, RB
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[J]. ANNALS OF HUMAN GENETICS, 1968, 31 : 401 - &