The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

Estrogen receptors and ischemic neuroprotection: Who, what, where, and when?

(2013) Derek A. Schreihofer et al.   BRAIN RESEARCH

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management

(2013) V. Nesbitt et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation

(2013) M. Mancuso et al.   NEUROLOGY

Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model

(2013) R. H. Hamalainen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation

(2012) Paul de Laat et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Oestrogens ameliorate mitochondrial dysfunction in Leber’s hereditary optic neuropathy

(2010) Carla Giordano et al.   BRAIN

Protean Phenotypic Features of the A3243G Mitochondrial DNA Mutation

(2009) Petra Kaufmann et al.   ARCHIVES OF NEUROLOGY

Diagnostic Approach to Mitochondrial Disorders: the Need for a Reliable Biomarker

(2009) M. Mancuso et al.   CURRENT MOLECULAR MEDICINE