Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation: importance of DNA collection for post-mortem diagnosis.

Authors

AL Gropman

Document Type

Journal Article

Publication Date

2011

Journal

Developmental Medicine & Child Neurology

Volume

53

Issue

2

Inclusive Pages

487-488

APA Citation

Gropman, A. (2011). Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation: importance of DNA collection for post-mortem diagnosis.. Developmental Medicine & Child Neurology, 53 (2). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_neuro_facpubs/820