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NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype |
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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: |
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Publisher: |
Elsevier Ltd |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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