SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation

被引:14
作者
Cascon, A. [1 ]
Cebrian, A. [1 ]
Ruiz-Llorente, S. [1 ]
Telleria, D. [1 ]
Benitez, J. [1 ]
Robledo, M. [1 ]
机构
[1] Spanish Natl Canc Ctr CNIO, Dept Human Genet, Madrid, Spain
关键词
D O I
10.1136/jmg.39.10.e64
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页数:3
相关论文
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