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1 patient data entry in database for mutations P587L and N864S.

Entry
#
Mutations
allele 1allele 2
Clinical representationSymptomsAge groupAge of onsetAge of patientAge of deathReference
24N864S1
T251I
P587L2
MNGIE-like, presented with GI symptoms, ptosis, neuropathy, muscle weakness.
-muscle weakness
-ptosis
juvenile
15n/an/aVan Goethem et al, 2003c;

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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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