Article ID Journal Published Year Pages File Type
8644330 European Journal of Medical Genetics 2018 23 Pages PDF
Abstract
To our knowledge, this is the first report describing a Libyan patient with dRTA who suffered from early-onset sensorineural hearing loss, with a digenic mode of inheritance, supported by the identification of two novel mutations. This study increases the understanding of how dRTA is genetically transmitted, while offers a good outline towards the molecular diagnostics and genetic counseling for dRTA in Lybians.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
Authors
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