ASPECIFIC MENTAL-RETARDATION AND HETEROZYGOSITY FOR PHENYLKETONURIA

被引：0
作者：
SARTORIO, R
VAJRO, P
DELGIUDICE, E
GRITTI, A
ANDRIA, G
机构：
[1] UNIV NAPLES,FAC MED & CHIRURG 2,PEDIAT CLIN,I-80134 NAPLES,ITALY
[2] UNIV NAPLES,FAC MED & CHIRURG 1,CATTEDRA NEUROPSICHIAT INFANTILE,I-80134 NAPLES,ITALY
来源：
RIVISTA ITALIANA DI PEDIATRIA-ITALIAN JOURNAL OF PEDIATRICS | 1982年 / 8卷 / 04期
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D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
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页码：651 / 652
页数：2
相关论文
共 3 条
[1]   GENETIC FAILURE OF FETAL AMINO-ACID JUSTIFICATION - COMMON BASIS FOR MANY FORMS OF METABOLIC, NUTRITIONAL, AND NONSPECIFIC MENTAL-RETARDATION [J].
BESSMAN, SP .
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[2]   RELATIVE INABILITY OF MOTHER AND CHILD TO CONVERT PHENYLALANINE TO TYROSINE - POSSIBLE CAUSE OF NONSPECIFIC MENTAL-RETARDATION [J].
FUJIMOTO, A ;
CRAWFORD, R ;
BESSMAN, SP .
BIOCHEMICAL MEDICINE, 1979, 21 (03) :271-276
[3]   CLASSIC PHENYLKETONURIA - DIAGNOSIS THROUGH HETEROZYGOTE DETECTION [J].
GRIFFIN, RF ;
ELSAS, LJ .
JOURNAL OF PEDIATRICS, 1975, 86 (04) :512-517
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