Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.
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| Description | scientific article |
| Author/s |
author: Anthony Robson Donna S. Mackay Dorothy Thompson Robert Henderson |
| Publication date | May 9, 2011 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |