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pro vyhledávání: '"Sharifah Ahmed Othman"'
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 3, Iss 1, Pp 36-40 (2020)
Background: Mitochondrial DNA-depletion syndromes (MDDS) usually present with a wide spectrum of clinical manifestations, such as weakness, hypotonia, developmental delay, and/or seizures, and are categorized as myopathic, encephalomyopathic, hepatoc
Externí odkaz:
https://doaj.org/article/2f0703f9774443e689ddecd73cfc67b7