Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges-Reference-Cited by-同舟云学术

Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges

Published:2021-07-15 Issue: Volume: Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Souissi Amal,Gibriel Abdullah A.,Masmoudi Saber

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00439-021-02314-y.pdf

Reference65 articles.

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2. Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H et al (2007) GJB2 (Connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation. Int J Pediatr Otorhinolaryngol 71(8):1239–1245. https://doi.org/10.1016/j.ijporl.2007.04.019

3. Ahmed ZM, Masmoudi S, Kalay E, Belyantseva IA, Mosrati MA, Collin RWJ, Riazuddin S et al (2008) Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet 40(11):1335–1340. https://doi.org/10.1038/ng.245

4. Ahmed ZM, Frolenkov G, Riazuddin S (2013) Usher proteins in inner ear structure and function. Physiol Genom 45(21):987–989. https://doi.org/10.1152/physiolgenomics.00135.2013

5. Ammar-Khodja F, Bonnet C, Dahmani M, Ouhab S, Lefèvre GM, Ibrahim H, Hardelin J-P, Weil D, Louha M, Petit C (2015) Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing. Mol Genet Genom Med 3(3):189–196. https://doi.org/10.1002/mgg3.131

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