Germ-line NF2 mutations and disease severity in neurofibromatosis type 2 patients with retinal abnormalities

被引:14
作者
Baser, ME
Kluwe, L
Mautner, VF
机构
[1] Univ Hosp Eppendorf, Hamburg, Germany
[2] Allgemeines Krankenhaus Ochsenzoll, Dept Neurol, Hamburg, Germany
关键词
D O I
10.1086/302338
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:1230 / 1233
页数:4
相关论文
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