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Publikováno v:
Neurologia i neurochirurgia polska. 48(2)
The A3243G mutation is one of the most frequent mutations of mitochondrial DNA. The phenotypic expression of the A3243G mutation is variable and causes a wide range of syndromic and non-syndromic clinical disorders. Mitochondrial myopathy, encephalop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e521c89a3ffa64a5fd481442b16c36e
https://pubmed.ncbi.nlm.nih.gov/24821643
https://pubmed.ncbi.nlm.nih.gov/24821643
