Novel mutation of human OCTN2 carnitine transporter in a patient with severe ischaemic heart disease

被引：0
|
作者：
Bene, J [1 ]
Komlósi, K [1 ]
Havasi, V [1 ]
Melegh, B [1 ]
机构：
[1] Univ Pecs, Dept Med Genet & Child Dev, Pecs, Hungary
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2002年 / 10卷
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D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
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页码：210 / 210
页数：1
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