NMNAT1 mutations cause Leber congenital amaurosis-Reference-Cited by-同舟云学术

NMNAT1 mutations cause Leber congenital amaurosis

Published:2012-07-29 Issue:9 Volume:44 Page:1040-1045
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Falk Marni J,Zhang Qi,Nakamaru-Ogiso Eiko,Kannabiran Chitra,Fonseca-Kelly Zoe,Chakarova Christina,Audo Isabelle,Mackay Donna S,Zeitz Christina,Borman Arundhati Dev,Staniszewska Magdalena,Shukla Rachna,Palavalli Lakshmi,Mohand-Said Saddek,Waseem Naushin H,Jalali Subhadra,Perin Juan C,Place Emily,Ostrovsky Julian,Xiao Rui,Bhattacharya Shomi S,Consugar Mark,Webster Andrew R,Sahel José-Alain,Moore Anthony T,Berson Eliot L,Liu Qin,Gai Xiaowu,Pierce Eric A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2361.pdf

Reference41 articles.

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3. den Hollander, A.I., Black, A., Bennett, J. & Cremers, F.P. Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. J. Clin. Invest. 120, 3042–3053 (2010).

4. Keen, T.J. et al. Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36. Eur. J. Hum. Genet. 11, 420–423 (2003).

5. Lau, C., Niere, M. & Ziegler, M. The NMN/NaMN adenylyltransferase (NMNAT) protein family. Front. Biosci. 14, 410–431 (2009).

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