A new PAX6 mutation in familial aniridia. |
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Authors: | I Hanson A Brown V van Heyningen |
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Affiliation: | MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK. |
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Abstract: | Aniridia (lack of iris) is caused by loss of function mutations in one copy of the PAX6 gene. Here we present a new PAX6 splice mutation in a family with autosomal dominant aniridia. The mutation is a single nucleotide change which, although occurring within an exon, affects the splice junction consensus and results in skipping of that exon. |
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