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Pomi Yun
Pediatric Neurology Residency · Johns Hopkins
Credentials: · · ·
History
Research
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Acta Neuropathologica · 2019 · 34 citations
International retrospective natural history study of LMNA-related congenital muscular dystrophy
Brain Communications · 2021 · 29 citations
Adult MTM1-related myopathy carriers: Classification based on deep phenotyping
Neurology · 2019 · 23 citations
16 papers
- PM
8 papers
7 papers
- JD
4 papers
- ML
4 papers
3 papers
3 papers
- SN
3 papers
