NMNAT1 E257K variant, associated with Leber Congenital...

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Experimental Eye Research 2018 / 4

NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype

Eblimit, Aiden, Zaneveld, Smriti Agrawal, Liu, Wei, Thomas, Kandace, Wang, Keqing, Li, Yumei, Mardon, Graeme, Chen, Rui
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Language:
english
Journal:
Experimental Eye Research
DOI:
10.1016/j.exer.2018.04.010
Date:
April, 2018
File:
PDF, 3.37 MB
english, 2018
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