Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndrome

Authors

F. Lacbawan
C.J. Tifft
N.L.C. Luban
S.M. Schmandt
M. Guerrera

Document Type

Journal Article

Publication Date

2000

Journal

American Journal of Medical Genetics

Volume

95

Inclusive Pages

266-268

Keywords

Pediatrics

APA Citation

Lacbawan, F., Tifft, C., Luban, N., Schmandt, S., & Guerrera, M. (2000). Clinical heterogeneity in mitochondrial DNA deletion disorders: a diagnostic challenge of Pearson syndrome. American Journal of Medical Genetics, 95 (). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/3523