2025/05/01 · 1 voice
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Genetic Neurodegenerative Diseases #Hereditary Neurological Disorders #Mitochondrial Function and Pathology
paper · pdf · doi:10.1242/dmm.052423
openalex publication_date 2025/05/01 · openalex created_date 2025/10/10 · openalex updated_date 2026/05/21
ABSTRACT First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping researchers promote themselves alongside their papers. Samia Pratt is first author on ‘ Evaluating the feasibility of gene replacement strategies to treat MTRFR deficiency’, published in DMM. Samia is a PhD student in the lab of Robert Burgess at The Jackson Laboratory, Bar Harbor, ME, USA, investigating potential gene therapeutics for rare inherited mitochondrial diseases and peripheral neuropathies.