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Autor:
Roy A.M. Haast, Dimo Ivanov, Rutger J.T. IJsselstein, Suzanne C.E.H. Sallevelt, Jacobus F.A. Jansen, Hubert J.M. Smeets, Irenaeus F.M. de Coo, Elia Formisano, Kâmil Uludağ
Publikováno v:
NeuroImage: Clinical, Vol 18, Iss , Pp 231-244 (2018)
One of the most common mitochondrial DNA (mtDNA) mutations, the A to G transition at base pair 3243, has been linked to changes in the brain, in addition to commonly observed hearing problems, diabetes and myopathy. However, a detailed quantitative d
Externí odkaz:
https://doaj.org/article/b57ab8f527354cf4a51efe3600c8d1a0