University research records
Pontifícia Universidade Católica de São Paulo
5 imported, source-linked research records. All imported publication dates.
All imported publication dates
Back to university profile →5 matching research records
Topic: Mitochondrial DNA mutations. Only records linked to Pontifícia Universidade Católica de São Paulo are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.
Showing 1–5 of 5 matching records. Counts update as records arrive.
mtDNA deletion m.8753_16566 with 10 % heteroplasmy in muscle and isolated complex-V dysfunction misinterpreted as chronic fatigue syndrome over 21-years
January 1, 2025 · 1 citations · Open access
Open original record →Mitochondrial small fiber neuropathy as a novel phenotypic trait of Leigh-like syndrome due to the variant m.10191T C in MT-ND3
January 1, 2023 · 2 citations · Open access
Open original record →Comment on “Proximal Myopathy due to m.5835G A Mutation in Mitochondrial MT-TY Gene”
July 1, 2019 · 0 citations · Open access
Open original record →Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance
September 1, 2008 · 9 citations · Open access
Open original record →Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients
February 1, 2006 · 47 citations · Open access
Open original record →
