Yazar "Safdar, Muhamad" için listeleme
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Association of a point mutation (m.9176T > G) of the MT-ATP6 gene with Leigh syndrome: A case report
Khailany, Rozhgar A.; Gilani, Naser; Özaslan, Mehmet; Safdar, Muhamad; Al-Shamari, Ihsan; Kanabe, Belan O.; Arslan, Ahmet (Biomedpress, 2020)Leigh Syndrome (LS) is an uncommon progressive neurodegenerative mitochondrial disorder. The condition is characterized by progressive mental and developmental disabilities (psychomotor regression) and commonly brings about ...