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1 patient data entry in database for mutation F961S.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
474F961S1
Mother of Japanese adPEO family. The proband, 69 years female, developed bilateral blepharoptosis and external ophthalmoplegia at forty. She also had slight muscle weakness and atrophy of proximal limbs and neck. Her mother, one of her three siblings and her daughter had same symptoms. Muscle biopsy examination of her and her brother showed several ragged red fibers.
-ragged red fibers
-muscle weakness
-ptosis
-PEO
-ophthalmoplegia
-external ophthalmoplegia
adult
4069n/aAdachi et al, 2002;

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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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