University research records
Mohamed I University
5 imported, source-linked research records. Open-access records.
Open-access records
Back to university profile →5 matching research records
Topic: Mitochondrial DNA mutations. Only records linked to Mohamed I University 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.
The human OPA1delTTAG mutation induces adult onset and progressive auditory neuropathy in mice
February 9, 2024 · 9 citations · Open access
Open original record →Autosomal recessive Leber hereditary optic neuropathy, a new neuro-ophthalmo-genetic paradigm
August 1, 2023 · 0 citations · Open access
Open original record →Autosomal recessive Leber hereditary optic neuropathy, a new neuro-ophthalmo-genetic paradigm
April 18, 2023 · 35 citations · Open access
Open original record →The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands
November 1, 2022 · 46 citations · Open access
Open original record →Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
September 1, 2022 · 7 citations · Open access
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