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 (Q43087850)
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scientific article published on 23 April 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article published on 23 April 2010 |
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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 (English)
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Peter Nürnberg
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Sibel Ugur Iseri
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Alexander W Wyatt
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Gudrun Nürnberg
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Christian Kluck
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Graham E Holder
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Ed Blair
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Alison Salt
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Nicola K Ragge
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23 April 2010
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