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Publications by Sara Shanske
Slowly Progressive Encephalopathy With Hearing Loss Due to a Mutation in the mtDNA tRNALeu(CUN) Gene
Journal of the Neurological Sciences
Neurology
Mutation in an mtDNA Protein-Coding Gene
Journal of Child Neurology
Child Health
Neurology
Pediatrics
Perinatology
A Novel mtDNA Deletion Associated With Primary Adrenal Insufficiency.† 594
Pediatric Research
Child Health
Pediatrics
Perinatology
Association of Mutations in SCO2, a Cytochrome C Oxidase Assembly Gene, With Early Fetal Lethality
Archives of Neurology
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