GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants - Concepedia

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

26

Citations

35

References

2018

Year

Mahbobeh Koohiyan, Morteza Hashemzadeh Chaleshtori, Mansoor Salehi, Hamidreza Abtahi, Somayeh Reiisi, Mohammad Reza Pourreza, Mohammad Reza Noori–Daloii, Mohammad Amin Tabatabaiefar

International Journal of Pediatric Otorhinolaryngology

Developmental BiologyIranian PopulationsNovel VariantsGenetic DisorderMendelian DisorderGeneticsGenetic EpidemiologyAudiologyGjb2 MutationsAuditory ResearchAuditory ScienceHuman HearingArtsMedicineHearing Loss

References

	Year	Citations

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