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

Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese families

(2010) Yinan Ma et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10

(2009) Carla S. Bergamin et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

The inheritance of pathogenic mitochondrial DNA mutations

(2009) L.M. Cree et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection

(2009) Rosetta Marotta et al.   JOURNAL OF CLINICAL NEUROSCIENCE

The study of mitochondrial A3243G mutation in different samples

(2009) Yinan Ma et al.   MITOCHONDRION

URINE HETEROPLASMY IS THE BEST PREDICTOR OF CLINICAL OUTCOME IN THE m.3243A>G mtDNA MUTATION

(2009) R. G. Whittaker et al.   NEUROLOGY

Macular Dystrophy Associated With the A3243G Mitochondrial DNA Mutation

(2008) Michel Michaelides   ARCHIVES OF OPHTHALMOLOGY

Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis

(2008) C. Verny et al.   DIABETES & METABOLISM