Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutation.
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| Description | scientific article published on 9 August 2016 |
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author: Simone Iwabe Sem Genini Luis Felipe Marinho Alexander Sumaroka Mychajlo S Kosyk Artur V Cideciyan Erin Scott Gustavo D Aguirre Samuel G. Jacobson Valerie Dufour Geoffrey Karl Aguirre |
| Publication date | August 9, 2016 |
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