Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis (Q93078250)
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scientific article published on 03 June 2019
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis |
scientific article published on 03 June 2019 |
Statements
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis (English)
Nejla Erkilic
Carla Sanjurjo-Soriano
Gaël Manes
Gregor Dubois
Christian P Hamel