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1 patient data entry in database for mutation S433C.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
595E1143G
S433C1
PEO, ataxia, peripheral neuropathy, and episodes of encephalopathy. Asymptomatic mother had also S433C.
-movement disorder (ataxia)
-peripheral neuropathy
-PEO
-encephalopathy
unknown
n/an/an/aHudson et al, 2006;

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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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