Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL-Reference-Cited by-同舟云学术

Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL

Published:2010-05-10 Issue:6 Volume:31 Page:
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Nichols Lorenzo L.¹,Alur Ramakrishna P.¹,Boobalan Elangovan¹,Sergeev Yuri V.¹,Caruso Rafael C.¹,Stone Edwin M.²³,Swaroop Anand⁴,Johnson Mary A.⁵,Brooks Brian P.¹

Affiliation:

1. Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland

2. Department of Ophthalmology, University of Iowa, Iowa City, Iowa

3. Howard Hughes Medical Institute, University of Iowa, Iowa City, Iowa

4. Neurobiology, Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland

5. Department of Ophthalmology and Visual Sciences, University of Maryland, Baltimore, Maryland

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.21268

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