Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness-Reference-Cited by-同舟云学术

Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness

Published:2023-03-16 Issue:9 Volume:280 Page:4057-4063
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Salame Malak,Bonnet Crystel,Moctar Ely Cheikh Mohamed,Brahim Selma Mohamed,Dedy Abdallahi,Vetah Ledour Abdel,Veten Fatimetou,Hamed Cheikh Tijani,Petit Christine,Houmeida Ahmed^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

https://link.springer.com/content/pdf/10.1007/s00405-023-07907-z.pdf

Reference29 articles.

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2. Sheffield AM, Smith RJ (2019) The epidemiology of deafness. Cold Spring Harb Perspect Med. https://doi.org/10.1101/cshperspect.a033258

3. Kimberly A, Gifford MD, Michael G, Holmes HH, Bernstein DO (2009) Hearing loss in children. Pediatr Rev 30(6):207–215. https://doi.org/10.1542/pir.30-6-207

4. Prasansuk S (2000) Incidence/prevalence of sensorineural hearing impairment in Thailand and Southeast Asia. Audiology 39(4):207–211. https://doi.org/10.3109/00206090009073080

5. Elahi MM, Elahi F, Elahi A, Elahi SB (1998) Paediatric hearing loss in rural Pakistan. J Otolaryngol 27(6):348–353

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