Results 121 to 130 of about 376,481 (188)

Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions. [PDF]

open access: yesFront Genet, 2022
Manini A   +11 more
europepmc   +1 more source

Carrier erythrocyte entrapped thymidine phosphorylase therapy for MNGIE [PDF]

open access: yes, 2008
Bax, BE   +11 more
core   +1 more source

[Mitochondrial encephalomyopathies].

open access: yesNihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 1995
L K, Hansen   +3 more
openaire   +3 more sources

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