MOLECULAR ANALYSIS OF THE INHERITANCE OF PHENYLKETONURIA AND MILD HYPERPHENYLALANINEMIA IN FAMILIES WITH BOTH DISORDERS

被引：48

作者：

LEDLEY, FD

LEVY, HL

WOO, SLC

机构：

[1] CHILDRENS HOSP MED CTR, INBORN ERRORS METAB PHENYLKETONURIA PROGRAM, BOSTON, MA 02115 USA

[2] MASSACHUSETTS GEN HOSP, NEUROL SERV, JOSEPH P KENNEDY LABS, BOSTON, MA 02114 USA

[3] HARVARD UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02115 USA

来源：

关键词：

D O I：

10.1056/NEJM198605153142002

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1276 / 1280

页数：5

共 31 条

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