Related content

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

By Annunen-Rasila Johanna   Finnilä Saara   Mykkänen Kati   Moilanen Jukka   Veijola Johanna   Pöyhönen Minna   Viitanen Matti   Kalimo Hannu   Majamaa Kari  

Neurogenetics, Vol. 7, Iss. 3, 2006-07 ,pp. : 185-194

Springer Publishing Company

Access to resources Recommend Favorite

Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders

By Lombès A.  

Brain, Vol. 124, Iss. 5, 2001-05 ,pp. : 984-994

Oxford University Press

Access to resources Recommend Favorite

Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G

By Kärppä Mikko   Mahjneh Ibrahim   Karttunen Ari   Tolonen Uolevi   Majamaa Kari  

Journal of Neurology, Vol. 251, Iss. 5, 2004-05 ,pp. : 556-563

Springer Publishing Company

Access to resources Recommend Favorite

Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA

By Kärppä Mikko  

Brain, Vol. 128, Iss. 8, 2005-08 ,pp. : 1861-1869

Oxford University Press

Access to resources Recommend Favorite

Frequencies of myohistological mitochondrial changes in patients with mitochondrial DNA deletions and the common m.3243A

By  

Neuropathology (Electronic), Vol. 35, Iss. 2, 2015-04 ,pp. : 130-136

John Wiley & Sons Inc

Access to resources Recommend Favorite