Paul T. Martin

This researcher's work centers on gene therapy approaches for genetic muscle diseases, including muscular dystrophy and GNE myopathy, using viral vectors (particularly AAV) to deliver corrective genes in animal models. Related work also explores glycosylation processes in muscle tissue and lysosomal storage disorders such as lysosomal acid lipase deficiency. Note that the publication list also includes some titles on unrelated topics (e.g., liver disease, lymphoma, psoriatic arthritis), which may reflect co-authorship on collaborative or multi-disciplinary studies rather than a core research focus.

Publication output has been variable over the last decade, with a dip in 2020 followed by fluctuating annual counts and a modest recent pace averaging about 2-3 papers per year.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026