MITOCHONDRIAL-DNA DELETION IN AN 8-YEAR-OLD BOY WITH PEARSON SYNDROME

被引：20

作者：

BAERLOCHER, KE

FELDGES, A

WEISSERT, M

SIMONSZ, HJ

ROTIG, A

机构：

[1] KANTONSSPITAL,EYE CLIN,CH-9007 ST GALLEN,SWITZERLAND

[2] HOP ENFANTS MALAD,PARIS,FRANCE

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1992年 / 15卷 / 03期

关键词：

D O I：

10.1007/BF02435968

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：327 / 330

页数：4

共 9 条

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[8] SITE-SPECIFIC DELETIONS OF THE MITOCHONDRIAL GENOME IN THE PEARSON MARROW PANCREAS SYNDROME [J].

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