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：
NEW ENGLAND JOURNAL OF MEDICINE | 1986年 / 314卷 / 20期
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
收藏
页码：1276 / 1280
页数：5
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