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A new PAX6 mutation in familial aniridia.
Authors:I Hanson   A Brown     V van Heyningen
Affiliation:MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
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.
Keywords:
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