Literature DB >> 12782766

Three novel PAX6 mutations in patients with aniridia.

W Zumkeller1, U Orth, A Gal.   

Abstract

AIMS: To describe mutations in the PAX6 gene in five patients with aniridia from three unrelated families.
METHODS: The PAX6 gene was analysed using single stranded conformational polymorphism analysis and direct sequencing.
RESULTS: In one family, three individuals from two generations had aniridia, whereas in each of the other families only one member was affected. The first patient had the heterozygous Q221X (1023C --> T) nonsense mutation in exon 8. The same mutation was found in his mother and sister. Another patient had a heterozygous Q297X (1252C --> T) mutation in exon 10. The third patient carried a heterozygous IVS5+2T --> C mutation leading to aberrant splicing of mRNA.
CONCLUSIONS: These findings provide further examples of haploinsufficiency of PAX6 in aniridia.

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Year:  2003        PMID: 12782766      PMCID: PMC1187315          DOI: 10.1136/mp.56.3.180

Source DB:  PubMed          Journal:  Mol Pathol        ISSN: 1366-8714


  19 in total

1.  Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region.

Authors:  C C Ton; H Hirvonen; H Miwa; M M Weil; P Monaghan; T Jordan; V van Heyningen; N D Hastie; H Meijers-Heijboer; M Drechsler
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

2.  PCR detection of 9 polymorphisms in the WT1 gene.

Authors:  K Tadokoro; N Oki; A Sakai; H Fujii; A Ohshima; S Nagafuchi; T Inoue; M Yamada
Journal:  Hum Mol Genet       Date:  1993-12       Impact factor: 6.150

3.  Human haploinsufficiency--one for sorrow, two for joy.

Authors:  E Fisher; P Scambler
Journal:  Nat Genet       Date:  1994-05       Impact factor: 38.330

4.  Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation).

Authors:  T Glaser; C C Ton; R Mueller; M L Petzl-Erler; C Oliver; N C Nevin; D E Housman; R L Maas
Journal:  Genomics       Date:  1994-01-01       Impact factor: 5.736

5.  Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene.

Authors:  T Glaser; D S Walton; R L Maas
Journal:  Nat Genet       Date:  1992-11       Impact factor: 38.330

6.  Aniridia. A review.

Authors:  L B Nelson; G L Spaeth; T S Nowinski; C E Margo; L Jackson
Journal:  Surv Ophthalmol       Date:  1984 May-Jun       Impact factor: 6.048

7.  Pax-6, a murine paired box gene, is expressed in the developing CNS.

Authors:  C Walther; P Gruss
Journal:  Development       Date:  1991-12       Impact factor: 6.868

8.  Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.

Authors:  I M Hanson; J M Fletcher; T Jordan; A Brown; D Taylor; R J Adams; H H Punnett; V van Heyningen
Journal:  Nat Genet       Date:  1994-02       Impact factor: 38.330

Review 9.  PAX6 mutations reviewed.

Authors:  J Prosser; V van Heyningen
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

10.  A new set of primers for mutation analysis of the human PAX6 gene.

Authors:  J Love; R Axton; A Churchill; V van Heyningen; I Hanson
Journal:  Hum Mutat       Date:  1998       Impact factor: 4.878

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  4 in total

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Review 4.  The Genetic and Endoplasmic Reticulum-Mediated Molecular Mechanisms of Primary Open-Angle Glaucoma.

Authors:  Wioletta Rozpędek-Kamińska; Radosław Wojtczak; Jacek P Szaflik; Jerzy Szaflik; Ireneusz Majsterek
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