Two new missense mutations (A105T and C110G) in the norrin gene in two Italian families with Norrie disease and familial exudative vitreoretinopathy

被引：0
|
作者：
Torrente, I
Mangino, M
Gennarelli, M
Novelli, G
Giannotti, A
Vadala, P
Dallapiccola, B
机构：
[1] UNIV ROMA TOR VERGATA,DIPARTIMENTO SANITA PUBBL & BIOL CELLULARE,CATTEDRA GENET UMANA & MED,I-00133 ROME,ITALY
[2] OSPED BAMBINE GESU,ROME,ITALY
[3] UNIV ROMA TOR VERGATA,CATTEDRA GENET MED,ROME,ITALY
[4] IST CSS LEUDEL,ROME,ITALY
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 72卷 / 02期
关键词：
D O I：
10.1002/(SICI)1096-8628(19971017)72:2<242::AID-AJMG23>3.0.CO;2-M
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：242 / 244
页数：3
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