Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) required for maintenance of the mammalian photoreceptor.

被引：0

作者：

Freund, CL

Bellingham, J

Furukawa, T

Looser, J

Herbrick, J

Scherer, S

Tsui, LC

Jacobson, S

Duncan, A

Papaioannou, M

Loutradis-Anagnostou, A

Bhattacharya, S

Cepko, C

Gregory-Evans, CY

McInnes, RR

机构：

[1] Hosp Sick Children, Toronto, ON M5G 1X8, Canada

[2] UCL, London WC1E 6BT, England

[3] Univ Penn, Philadelphia, PA 19104 USA

[4] Harvard Univ, Sch Med, Boston, MA USA

[5] Queens Univ, Kingston, ON K7L 3N6, Canada

[6] Ctr Thalassemia, Athens, Greece

来源：

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：A20 / A20

页数：1