Cavatina K. Truong

Molecular and clinical genetics of mitochondrial diseases due to<i>POLG</i>mutations

Lee-Jun Wong, Robert K. Naviaux, Nicola Brunetti‐Pierri et al. · Human Mutation · 2008 · 287 citations · Full text

Genetics, Molecular Genetics, Disease Gene Identification +18

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase

David Dimmock, Q. Zhang, Carlo Dionisi‐Vici et al. · Human Mutation · 2008 · 167 citations · Full text

Deoxyguanosine Kinase, Dna Damage, Genetics +18

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders

Hong Cui, Fangyuan Li, David Chen et al. · Genetics in Medicine · 2013 · 131 citations · Full text

Mitochondrial Myopathy, Dna, Mendelian Disorder +13

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy

Lee-Jun Wong, Nicola Brunetti‐Pierri, Qing Zhang et al. · Hepatology · 2007 · 115 citations

The pharmacogenetics and pharmacogenomics knowledge base: accentuating the knowledge

Tina Hernandez‐Boussard, Michelle Whirl‐Carrillo, Joan M. Hebert et al. · Nucleic Acids Research · 2007 · 109 citations · Full text

Genetics, Genetic Epidemiology, Bioinformatics Database +17