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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hearing Loss and LRTOMT[original query]
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
Analysis of p.Gly12Valfs*2, p.Trp24* and p.Trp77Arg mutations in GJB2 and p.Arg81Gln variant in LRTOMT among non syndromic hearing loss Egyptian patients: implications for genetic diagnosis.
Molecular biology reports 2019 Feb .
Gibriel Abdullah A, Abou-Elew Maha H, Masmoudi Sab
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
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