Novel mutations in the gene encoding alanine: Glyoxylate aminotransferase (AGT) causing primary hyperoxaluria type I (PH1).

被引：0
|
作者：
Rinat, C [1 ]
Drukker, A [1 ]
Frishberg, Y [1 ]
机构：
[1] SHAARE ZEDEK MED CTR, JERUSALEM, ISRAEL
来源：
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 1997年 / 8卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：A1825 / A1825
页数：1
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