Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA

被引：5
|
作者：
Van Goethem, G
Löfgren, A
Martin, JJ
Van Broeckhoven, C
机构：
[1] Univ Instelling Antwerp, Dept Biochem, Mol Genet Lab, Born Bunge Fdn,Neurogenet Grp, B-2610 Antwerp, Belgium
[2] Univ Instelling Antwerp, Dept Med, Neuropathol Lab, Born Bunge Fdn, B-2610 Antwerp, Belgium
[3] Univ Instelling Antwerp VIB, Born Bunge Fdn, B-2610 Antwerp, Belgium
[4] Univ Antwerp Hosp, Div Neurol, Antwerp, Belgium
来源：
JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷 / 07期
关键词：
D O I：
10.1136/jmg.37.7.547
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：547 / 548
页数：2
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