A new mutation of Wilson's disease p-type ATPase gene in a patient with cirrhosis and coombs-positive hemolytic anemia

被引：9
|
作者：
Leggio, L
Addolorato, G
Loudianos, G
Abenavoli, L
Lepori, M
Vecchio, FM
Rapaccini, GL
De Virgiliis, S
Gasbarrini, G
机构：
[1] Univ Cattolica Sacro Cuore, Inst Internal Med, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Inst Pathol, I-00168 Rome, Italy
[3] Osped Reg Microcitemie Cagliari, Cagliari, Italy
[4] CNR, Inst Neurogenet & Neuropharmacol, Cagliari, Italy
[5] Univ Cagliari, Dept Biomed Sci & Biotechnol, Cagliari, Italy
来源：
DIGESTIVE DISEASES AND SCIENCES | 2006年 / 51卷 / 01期
关键词：
Wilson's disease; homozygote mutation; genotype; phenotype;
D O I：
10.1007/s10620-006-3080-8
中图分类号：
R57 [消化系及腹部疾病];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：34 / 38
页数：5
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