Work

Clinical Heterogeneity in Mitochondrial DNA Deletion Disorders: A Diagnostic Challenge of Pearson Syndrome

Year: 2000

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/1096-8628(20001127)95:3<266::aid-ajmg13>3.0.co;2-0

Authors: Felicitas Lacbawan, Cynthia J. Tifft, Naomi L.C. Luban, Susanne M. Schmandt, Michael Guerrera, Steven Weinstein, Mark Pennybacker, Lee-Jun C. Wong

Institutions: National Institutes of Health, Children's National, National Human Genome Research Institute, Georgetown University Medical Center

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

OpenAlex ID: W1992421367

FWCI: 0.68

Cites: 18

Cited by: 45

Related to: 10