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                                       Details for article 15 of 19 found articles
 
 
  NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype
 
 
Title: NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype
Author: Eblimit, Aiden
Zaneveld, Smriti Agrawal
Liu, Wei
Thomas, Kandace
Wang, Keqing
Li, Yumei
Mardon, Graeme
Chen, Rui
Appeared in: Experimental eye research
Paging: Volume 173 (2018) nr. C pages 32-43
Year: 2018
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 15 of 19 found articles
 
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