University research records

Pontifícia Universidade Católica de São Paulo

5 imported, source-linked research records. Open-access records.

Open-access records

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.

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Showing 1–5 of 5 matching records. Counts update as records arrive.

  1. 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

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  2. 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

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  3. Comment on “Proximal Myopathy due to m.5835G A Mutation in Mitochondrial MT-TY Gene”

    July 1, 2019 · 0 citations · Open access

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  4. Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance

    September 1, 2008 · 9 citations · Open access

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  5. Prevalence of the A1555G (12S rRNA) and tRNA Ser(UCN) mitochondrial mutations in hearing-impaired Brazilian patients

    February 1, 2006 · 47 citations · Open access

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