Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Deafness and LRTOMT[original query] |
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The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population. Molecular biology reports 2012 Dec 39 (12): 11011-6. Charif Majida, Bounaceur Safaa, Abidi Omar, Nahili Halima, Rouba Hassan, Kandil Mostafa, Boulouiz Redouane, Barakat Abdelham |
Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss. International journal of molecular and cellular medicine 2013 2 (1): 41-5. Taghizadeh Seyyed Hossein, Kazeminezhad Seyyed Reza, Sefidgar Seyyed Ali Asghar, Yazdanpanahi Nasrin, Tabatabaeifar Mohammad Amin, Yousefi Ahmad, Lesani Seyyed Mohammad, Abolhasani Marziyeh, Hashemzadeh Chaleshtori Morte |
Deep analysis of the LRTOMTc.242G>A variant in non-syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies. Molecular genetics & genomic medicine 2021 9 9 (10): e1810. Mosrati Mohamed Ali, Fadhlaoui-Zid Karima, Benammar-Elgaaied Amel, Gibriel Abdullah Ahmed, Ben Said Mariem, Masmoudi Sab |
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2023 3 . Salame Malak, Bonnet Crystel, Moctar Ely Cheikh Mohamed, Brahim Selma Mohamed, Dedy Abdallahi, Vetah Ledour Abdel, Veten Fatimetou, Hamed Cheikh Tijani, Petit Christine, Houmeida Ahm |
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