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2 patient data entries in database for clusters A467T and A467T in age group "infantile". Entry
# | | Mutations | | allele 1 | allele 2 |
| Clinical representation | Symptoms | Age group | Age of onset | Age of patient | Age of death | Reference | | | 289 | A467T2
| A467T2
| Developemental delay, status epilepticus onset, valproic acid therapy 2 weeks, epilepsia partialis continua, mtDNA depletion in liver | | | 2.67 | 6 | n/a | Wolf et al, 2009; [view data] | | 522 | A467T2
| A467T2
| Alpers, Encephalopathy, liver failure. | | | 1 | n/a | n/a | Stewart et al, 2009; [view data] |
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. Number of displayed patient cases: 2
Avg age of onset in displayed cases: 1.8
Std dev in onset in displayed cases: 0.8
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