Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration-Reference-Cited by-同舟云学术

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Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

Published:2004-06-30 Issue:17 Volume:13 Page:1893-1902
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Jacobson S. G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/13/17/1893/6948711/ddh198.pdf

Cited by 92 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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3. NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal development;Journal of Clinical Investigation;2024-04-23

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