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Mutations on the Protein: P12235 From Positions: 283 To 298

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1
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Swiss-Prot Disease: VAR_012112
p.VAL289MET
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 2 (PEOA2)


OMIM Disease: 103220.0002
p.VAL289MET
N/A
N/A
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL DOMINANT, 2






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