The mitochondrial DNA A3243G mutation in Portugal:clinical and molecular studies in 5 families.
Articolo
Data di Pubblicazione:
1999
Abstract:
This study, the first in Portuguese patients, confirms the frequent occurrence of the A3243G mutation in patients with mitochondrial diseases, and emphasises the usefulness of genetic testing in reaching a correct diagnosis.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
migraine; genetics; aura; mitochondrial diseases
Elenco autori:
Vilarinho, L.; Santorelli, F. M.; Coelho, I.; Rodriques, I.; Maia, M.; Barata, I.; Cabral, P.; Dionisio, A.; Costa, Alfredo; Guimares, A.; Di Mauro, S.
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