Literature DB >> 17627385

Application of dHPLC for mutation detection of the fibrillin-1 gene for the diagnosis of Marfan syndrome in a National Health Service Laboratory.

Rachel Howarth1, Catharina Yearwood, John F Harvey.   

Abstract

Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder caused by mutations in the fibrillin-1 gene FBN1. Mutation detection of this 65-exon gene presents a particular challenge for the diagnostic service in cost, time constraints, and the need to maintain a stringently optimized assay procedure. Using denaturing high-performance liquid chromatography (dHPLC), we have designed a procedure for rapid mutation scanning, redesigning 50% of published primer sets, screening by Ensembl to avoid inclusion of polymorphic variations and employing a limited set of PCR conditions to allow for a high-throughput 96-well format. We have screened 262 unrelated patients with MFS or Marfan-like phenotypes and detected 103 (39.3%) mutations including 93 different mutations, 72 of which are novel. The mutations include 55 missense (53.4%) 19 splice site (18.5%), 17 frameshift (16.5%), 11 nonsense (10.7%) and 1 in-frame deletion/insertion.

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Year:  2007        PMID: 17627385     DOI: 10.1089/gte.2006.0514

Source DB:  PubMed          Journal:  Genet Test        ISSN: 1090-6576


  9 in total

1.  Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events.

Authors:  Linnea M Baudhuin; Katrina E Kotzer; Susan A Lagerstedt
Journal:  Genet Med       Date:  2014-08-07       Impact factor: 8.822

2.  Sensitive genotyping of mutations in the EGFR gene from NSCLC patients using PCR-GoldMag lateral flow device.

Authors:  Xian-Ying Li; Chao Zhang; Qin-Lu Zhang; Juan-Li Zhu; Qian Liu; Ming-Wei Chen; Xue-Min Yang; Wen-Li Hui; Ya-Li Cui
Journal:  Sci Rep       Date:  2017-08-21       Impact factor: 4.379

3.  Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet-Biedl Syndrome-Like Phenotype.

Authors:  Maria Luce Genovesi; Barbara Torres; Marina Goldoni; Eliana Salvo; Claudia Cesario; Massimo Majolo; Tommaso Mazza; Carmelo Piscopo; Laura Bernardini
Journal:  Front Genet       Date:  2022-07-15       Impact factor: 4.772

4.  New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome.

Authors:  Ren-Qiang Yang; Javad Jabbari; Xiao-Shu Cheng; Reza Jabbari; Jonas B Nielsen; Bjarke Risgaard; Xu Chen; Ahmad Sajadieh; Stig Haunsø; Jesper Hastrup Svendsen; Morten S Olesen; Jacob Tfelt-Hansen
Journal:  BMC Genet       Date:  2014-06-18       Impact factor: 2.797

5.  Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis.

Authors:  Jie Li; Xiaoyun Jia; Shiqiang Li; Shaohua Fang; Xiangming Guo
Journal:  Mol Vis       Date:  2014-07-18       Impact factor: 2.367

6.  Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.

Authors:  J K Poninska; Z T Bilinska; M Franaszczyk; E Michalak; M Rydzanicz; E Szpakowski; A Pollak; B Milanowska; G Truszkowska; P Chmielewski; A Sioma; H Janaszek-Sitkowska; A Klisiewicz; I Michalowska; M Makowiecka-Ciesla; P Kolsut; P Stawinski; B Foss-Nieradko; M Szperl; J Grzybowski; P Hoffman; A Januszewicz; M Kusmierczyk; R Ploski
Journal:  J Transl Med       Date:  2016-05-04       Impact factor: 5.531

7.  Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype.

Authors:  Elena Sticchi; Rosina De Cario; Alberto Magi; Sabrina Giglio; Aldesia Provenzano; Stefano Nistri; Guglielmina Pepe; Betti Giusti
Journal:  Biomed Res Int       Date:  2018-09-05       Impact factor: 3.411

8.  Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders.

Authors:  Eline Overwater; Luisa Marsili; Marieke J H Baars; Annette F Baas; Irma van de Beek; Eelco Dulfer; Johanna M van Hagen; Yvonne Hilhorst-Hofstee; Marlies Kempers; Ingrid P Krapels; Leonie A Menke; Judith M A Verhagen; Kak K Yeung; Petra J G Zwijnenburg; Maarten Groenink; Peter van Rijn; Marjan M Weiss; Els Voorhoeve; J Peter van Tintelen; Arjan C Houweling; Alessandra Maugeri
Journal:  Hum Mutat       Date:  2018-07-12       Impact factor: 4.878

Review 9.  The Molecular Genetics of Marfan Syndrome.

Authors:  Qiu Du; Dingding Zhang; Yue Zhuang; Qiongrong Xia; Taishen Wen; Haiping Jia
Journal:  Int J Med Sci       Date:  2021-05-27       Impact factor: 3.738

  9 in total

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