Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans-Reference-Cited by-同舟云学术

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Published:2008-10-26 Issue:11 Volume:40 Page:1335-1340
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ahmed Zubair M,Masmoudi Saber,Kalay Ersan,Belyantseva Inna A,Mosrati Mohamed Ali,Collin Rob W J,Riazuddin Saima,Hmani-Aifa Mounira,Venselaar Hanka,Kawar Mayya N,Tlili Abdelaziz,van der Zwaag Bert,Khan Shahid Y,Ayadi Leila,Riazuddin S Amer,Morell Robert J,Griffith Andrew J,Charfedine Ilhem,Çaylan Refik,Oostrik Jaap,Karaguzel Ahmet,Ghorbel Abdelmonem,Riazuddin Sheikh,Friedman Thomas B,Ayadi Hammadi,Kremer Hannie

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.245.pdf

Reference30 articles.

1. Friedman, T.B. & Griffith, A.J. Human nonsyndromic sensorineural deafness. Annu. Rev. Genomics Hum. Genet. 4, 341–402 (2003).

2. Grant, L. & Fuchs, P.A. Auditory transduction in the mouse. Pflugers Arch. 454, 793–804 (2007).

3. Morton, C.C. & Nance, W.E. Newborn hearing screening–a silent revolution. N. Engl. J. Med. 354, 2151–2164 (2006).

4. Pasek, S., Risler, J.L. & Brezellec, P. Gene fusion/fission is a major contributor to evolution of multi-domain bacterial proteins. Bioinformatics 22, 1418–1423 (2006).

5. Kalay, E. et al. A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4. J. Mol. Med. 85, 397–404 (2007).

Cited by 61 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. Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health;Frontiers in Genetics;2024-04-22

2. Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades;Journal of Cellular and Molecular Medicine;2024-03-27

3. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis;International Journal of Pediatric Otorhinolaryngology;2023-05

4. Mechanoelectrical transduction-related genetic forms of hearing loss;Current Opinion in Physiology;2023-04

5. Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness;European Archives of Oto-Rhino-Laryngology;2023-03-16