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Additional file 1: of Investigation of SLA4A3 as a candidate gene for human retinal disease

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posted on 2016-05-23, 05:00 authored by Louise Downs, Andrew Webster, Anthony Moore, Michel Michaelides, Robin Ali, Alison Hardcastle, Cathryn Mellersh
Molecularly unsolved patients with autozygosity data indicating a homozygous region containing SLC4A3. In eight of the individuals studied, previous autozygosity mapping had identified loci associated with retinal disease. Here we list the sizes of the loci and the number of genes in each. (PDF 16 kb)

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Guide Dogs for the Blind Association

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    Springer Nature

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    SLC4A3Retinitis pigmentosaRetinal degeneration

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