CLINICAL, BIOCHEMICAL, AND MOLECULAR GENETIC ANALYSES OF HUMAN MITHOCHONDRIAL CARDIOMYOPATHIES
- 2 Anni 1996/1998
- 61.975€ Totale Fondi
Descrizione non disponibile
Pubblicazioni Scientifiche
- 1999-01-01 AMERICAN JOURNAL OF HUMAN GENETICS
Maternally inherited cardiomyopathy: An atypical presentation of the mtDNA 12S rRNA gene A1555G mutation
- 1999-12-01 EUROPEAN JOURNAL OF HUMAN GENETICS
MtDNA-related idiopathic dilated cardiomyopathy
- 1998-05-01 MUSCLE & NERVE
Genetic heterogeneity of myoclonus epilepsy with ragged-red fibers syndrome
- 1999-03-23 NEUROLOGY
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family
- 2001-03-27 NEUROLOGY
Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a sephardic Jewish family
- 1997-05-01 NEUROMUSCULAR DISORDERS
Mitochondrial tRNA(Cys) gene mutation (A5814G): A second family with mitochondrial encephalopathy
