Super-resolution microscopy reveals photoreceptor-specific subciliary location and function of ciliopathy-associated protein CEP290
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/145256/files/pdf
Reference83 articles.
1. The Ciliopathies: An Emerging Class of Human Genetic Disorders
2. Genetic Defects in Ciliary Structure and Function
3. Photoreceptor Cilia and Retinal Ciliopathies
4. Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
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