Hanson I, Brown A, van Heyningen V
MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.
J Med Genet. 1995 Jun;32(6):488-9. doi: 10.1136/jmg.32.6.488.
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.
无虹膜症(虹膜缺失)是由PAX6基因一个拷贝的功能丧失性突变引起的。在此,我们报告了一个常染色体显性遗传无虹膜症家族中的一种新的PAX6剪接突变。该突变是单个核苷酸的改变,尽管发生在外显子内,但影响剪接位点的一致性,导致该外显子缺失。