Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation
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| Description | scientific article |
| Author/s |
author: Ola Sandgren Irina Golovleva |
| Publication date | March 9, 2012 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |