A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double‐strand breaks in yeast-Reference-Cited by-同舟云学术

A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double‐strand breaks in yeast

Published:2006-08-04 Issue:11 Volume:20 Page:1910-1912
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Sironi Manuela¹²,Pozzoli Uberto¹,Comi Giacomo P.³,Riva Stefania¹,Bordoni Andreina³,Bresolin Nereo¹³,Nag Dilip K.²⁴,Sironi Manuela¹²,Pozzoli Uberto¹,Comi Giacomo P.³,Riva Stefania¹,Bordoni Andreina³,Bresolin Nereo¹³,Nag Dilip K.²⁴

Affiliation:

1. Scientific Institute IRCCS E. MedeaBosisio Parini (LC)Italy

2. Molecular Genetics ProgramCenter for Medical SciencesWadsworth CenterAlbanyNew YorkUSA

3. Dino Ferrari CentreDepartment of Neurological SciencesUniversity of MilanIRCCS Ospedale Maggiore PoliclinicoMangiagalli and Regina Elena FoundationMilanItaly

4. Department of Biomedical SciencesSchool of Public HealthState University of New YorkAlbanyNew YorkUSA

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.05-5635fje

Reference45 articles.

1. Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.

2. Initial sequencing and analysis of the human genome

3. The structural and functional diversity of dystrophin

4. Topography of the Duchenne muscular dystrophy(DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen J. T.;Am. J. Hum. Genet.,1989

5. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion;Koenig M.;Am. J. Hum. Genet.,1989

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Next-generation sequencing approach to molecular diagnosis of Iranian patients with Duchenne/Becker muscular dystrophy: Several novel variants identified;eNeurologicalSci;2023-03

2. Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy;Current Gene Therapy;2018-01-04

3. Diagnosis of Inherited Neuromuscular Disorders by Next-Generation–Sequencing;SpringerBriefs in Genetics;2013

4. Exon skipping for nonsense mutations in Duchenne muscular dystrophy: too many mutations, too few patients?;Expert Opinion on Biological Therapy;2012-06

5. Detection of truncated dystrophin lacking the C-terminal domain in a Chinese pedigree by next-generation sequencing;Gene;2012-05