Assignment of Ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridization

被引：0
|
作者：
Gasparini, P [1 ]
Calvano, S [1 ]
Memeo, E [1 ]
Bisceglia, L [1 ]
Zelante, L [1 ]
机构：
[1] Osped CSS, IRCCS, Serv Genet Med, I-71013 San Giovanni Rotondo, Italy
来源：
ANNALES DE GENETIQUE | 1997年 / 40卷 / 04期
关键词：
FTL gene; FISH localisation;
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
A new genetic disorder (Hyperferritinemia and Cataract Syndrome) characterized by a combination of high serum ferritin level and congenital bilateral nuclear cataract has been recently described. This disease is trasmitted as autosomal dominant trait and is due to mutations in the ferritin L gene (FTL). FTL gene has been localized to 19q13.3-qter by somatic cell hybrids. In this work we present the precise mapping of FTL gene on chromosome 19q13.3 using in situ fluorescence hybridization.
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收藏
页码：227 / 228
页数：2
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