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Mutations on the Protein: P54098 From Positions: 681 To 743

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1
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Swiss-Prot Disease: VAR_058885
p.GLY737ARG
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB)


OMIM Disease: 174763.0019
p.GLY737ARG
N/A
N/A
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,||AUTOSOMAL RECESSIVE






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