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1 patient data entry in database for mutations R309L and Q968E.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
653Q968E
R309L3
progressive external ophthalmoplegia (PEO) and negative family history. At the age of 38, she observed impaired eye movements and ptosis. Skeletal muscle biopsy disclosed ragged red fibres. Multiple mtDNA deletions were present in muscle tissue.
-ragged red fibers
-ptosis
-PEO
-ophthalmoplegia
-external ophthalmoplegia
adult
3854n/aKaliszewska et al, 2015;

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1-5 pathogenic cluster assignment of mutations. Mutations displayed without a superscript number are outside of the assigned pathogenic clusters. See cluster definitions for details.

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Use "PNF" for non-missense mutations.
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