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1 patient data entry in database for mutations W748S and P1073L.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
177P1073L3
W748S5
Psychomotor delay, status epilepticus, liver disease, lactic acidosis, ADHD, mental retardation.
-lactic acidosis
-status epilepticus
-liver dysfunction
-psychomotor delay
-retardation
infantile
0.01n/a13Kurt et al, 2010;

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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.

Search criteria for patient entries:
Mutations Entry IDs Clusters Reference Residue range
Mutations:
Allele 1:Allele 2:
Separate multiple mutations with commas.
Use "PNF" for non-missense mutations.
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