FAMILIAL HYPERPROLINEMIA - REPORT OF A 2ND CASE ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION WITH DEMONSTRATION OF AN ENZYME DEFECT

被引:120
作者
EFRON, ML
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D O I
10.1056/NEJM196506172722401
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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页码:1243 / +
页数:1
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