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Mutations on the Protein: P54098 From Positions: 372 To 434

2
2
0
0


Swiss-Prot Disease: VAR_058876
p.GLY380ASP
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB)


Swiss-Prot Disease: VAR_023667
p.GLY431VAL
N/A
N/A
Progressive external ophthalmoplegia with mitochondrial DNA deletions autosomal recessive (PEOB)






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