A South African family with the mitochondrial A1555G mutation on haplogroup L0d
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
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1. High prevalence of m.1555A > G in patients with hearing loss in the Baikal Lake region of Russia as a result of founder effect;Scientific Reports;2024-07-03
2. Screening of A1555G mDNA Variant Using U-TOP™HL Genotyping Kit in Korean Family with Progressive Hearing Loss;Korean Journal of Otorhinolaryngology-Head and Neck Surgery;2021-02-21
3. Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: A report from Nigeria;International Journal of Pediatric Otorhinolaryngology;2014-11
4. Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation;BMC Genetics;2014-02-17
5. Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population;International Journal of Pediatric Otorhinolaryngology;2011-05
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