Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy
| Image |  |
|---|---|
| Description | scientific article published on 23 April 2010 |
| Author/s |
author: Peter Nürnberg |
| Publication date | April 23, 2010 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |