LESCH-NYHAN SYNDROME IN AN ARAB FAMILY - DETECTION AND BIOCHEMICAL MANIFESTATION OF HETEROZYGOSITY

被引：0
|
作者：
SHALTIEL, A
KATZUNI, E
BOER, P
ZOREFSHANI, E
SPERLING, O
机构：
[1] BEILINSON MED CTR,DEPT CLIN BIOCHEM,I-49100 PETAH TIKVA,ISRAEL
[2] CENT EMEK HOSP,DEPT PEDIAT B,AFULA,ISRAEL
[3] TEL AVIV UNIV,SACKLER SCH MED,TEL AVIV,ISRAEL
[4] CHAIM SHEBA MED CTR,DEPT CHEM PATHOL,TEL HASHOMER,ISRAEL
来源：
ISRAEL JOURNAL OF MEDICAL SCIENCES | 1981年 / 17卷 / 12期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：1169 / 1173
页数：5
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