Work

Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA

Year: 2001

Type: review

Source: Seminars in Cell and Developmental Biology

DOI: 10.1006/scdb.2001.0279

Authors: Michio Hirano, Ramon Marti, Claudia Ferreiro-Barros, Maya R Vilà, Saba Tadesse, Yutaka Nishigaki, Ichizo Nishino, Tuan H Vu

Institutions: Columbia University Irving Medical Center, Columbia University, National Center of Neurology and Psychiatry, National Institute of Neuroscience

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: MITOCHONDRIAL DNA MUTATIONS IN HUMAN CARDIOMYOPATHIES, MOLECULAR PATHOGENESIS OF MNGIE SYNDROME, MITOCHONDRIAL DNA DEPLETION IN HUMAN DISEASE

OpenAlex ID: W2026293800

FWCI: 1.025

Cites: 94

Cited by: 109

Related to: 10