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

Concepedia

Publication | Open Access

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

DOI Full Paper Access

84

Citations

24

References

2008

Year

Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay, Inna A. Belyantseva, Mohamed Ali Mosrati, Rob W.J. Collin, Saima Riazuddin, Mounira Hmani‐Aifa, Hanka Venselaar, Mayya N Kawar,

Nature Genetics

Nonsyndromic DeafnessMendelian DisorderGenetic DisorderGeneticsAudiologyAlternative Reading FramesMolecular GeneticsFusion GeneCochlear DevelopmentArtsMedicineHearing Loss

References

	Year	Citations

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