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1 patient data entry in database for mutation E895G.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
196E895G1
Found in one newborn with floppiness and 20% liver mtDNA depletion- Myopathic MDS. Death at 36 hours after birth. 5% mtDNA copy number in muscle, 20% mtDNA copy number in liver.
-no known symptoms
infantile
0.01n/a0.02Spinazzola et al, 2009;

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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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