Literature DB >> 2575483

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.

M Mannens1, E M Bleeker-Wagemakers, J Bliek, J Hoovers, I Mandjes, S van Tol, R R Frants, C Heyting, A Westerveld, R M Slater.   

Abstract

In a large pedigree with autosomal dominant aniridia, we found close linkage between the aniridia locus AN2 and the markers catalase (CAT) (zeta = 7.27 at theta = 0.00) and D11S151 (zeta = 3.86 at theta = 0.10) flanking the AN2 locus on 11p13. Positive lod scores were also obtained for the 11p13----11p14 markers D11S16 and FSHB with the linkage group CAT/AN2/D11S151. We conclude that the autosomal dominant aniridia in this family is due to a mutation at the AN2 locus on 11p13. We have excluded linkage (zeta less than -2 at theta less than 0.18) between the aniridia and the chromosome 2p25 marker D2S1 (linked to ACP1).

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Year:  1989        PMID: 2575483     DOI: 10.1159/000132834

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  10 in total

1.  Congenital aniridia: long-term clinical course, visual outcome, and prognostic factors.

Authors:  Ji Woong Chang; Jeong Hun Kim; Seong-Joon Kim; Young Suk Yu
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2.  Phenotypic severity scoring system and categorisation for prune belly syndrome: application to a pilot cohort of 50 living patients.

Authors:  Daniel G Wong; Michelle K Arevalo; Niccolo Maria Passoni; Nida S Iqbal; Thomas Jascur; Adam J Kern; Emma J Sanchez; Arthi Satyanarayan; Jyothsna Gattineni; Linda A Baker
Journal:  BJU Int       Date:  2018-09-19       Impact factor: 5.588

Review 3.  The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities-A review.

Authors:  Inas F Aboobakar; Janey L Wiggs
Journal:  Clin Exp Ophthalmol       Date:  2022-01-17       Impact factor: 4.383

Review 4.  Aniridia: recent achievements in paediatric practice.

Authors:  I Ivanov; A Shuper; M Shohat; M Snir; R Weitz
Journal:  Eur J Pediatr       Date:  1995-10       Impact factor: 3.183

5.  Detection of a cryptic paracentric inversion within band 11p13 in familial aniridia by fluorescence in situ hybridization.

Authors:  Y Fukushima; J Hoovers; M Mannens; K Wakui; H Ohashi; T Ohno; Y Ueoka; N Niikawa
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

6.  Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.

Authors:  M Drechsler; E J Meijers-Heijboer; S Schneider; B Schurich; C Grond-Ginsbach; G Tariverdian; G Kantner; A Blankenagel; D Kaps; T Schroeder-Kurth
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

7.  Mutation of the PAX6 gene in patients with autosomal dominant keratitis.

Authors:  F Mirzayans; W G Pearce; I M MacDonald; M A Walter
Journal:  Am J Hum Genet       Date:  1995-09       Impact factor: 11.025

8.  A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family.

Authors:  Chongfei Jin; Qiwei Wang; Jinyu Li; Yanan Zhu; Xingchao Shentu; Ke Yao
Journal:  Mol Vis       Date:  2012-02-16       Impact factor: 2.367

9.  PAX6 aniridia and interhemispheric brain anomalies.

Authors:  Hana Abouzeid; Mohamed A Youssef; Nihal ElShakankiri; Philippe Hauser; Francis L Munier; Daniel F Schorderet
Journal:  Mol Vis       Date:  2009-10-17       Impact factor: 2.367

10.  Mutation analysis of paired box 6 gene in inherited aniridia in northern China.

Authors:  Peng Chen; Xinjie Zang; Dapeng Sun; Ye Wang; Yao Wang; Xiaowen Zhao; Mohan Zhang; Lixin Xie
Journal:  Mol Vis       Date:  2013-05-30       Impact factor: 2.367

  10 in total

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