5 NOVEL MISSENSE MUTATIONS OF THE PHENYLALANINE-HYDROXYLASE GENE IN PHENYLKETONURIA

被引：9

作者：

BENIT, P ^{[1
]}

REY, F ^{[1
]}

MELLE, D ^{[1
]}

MUNNICH, A ^{[1
]}

REY, J ^{[1
]}

机构：

[1] HOP NECKER ENFANTS MALAD, INSERM, U393, UNITE RECH HANDICAPS GENET ENFANT, F-75743 PARIS, FRANCE

来源：

关键词：

D O I：

10.1002/humu.1380040311

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：229 / 231

页数：3

共 12 条

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[7] Kaufman S., 1976, ADV NEUROCHEM, P1
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[9] MOLECULAR-BASIS OF PHENOTYPIC HETEROGENEITY IN PHENYLKETONURIA
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