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：

引用

页码：A1825 / A1825

页数：1

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