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Mutations on the Protein: P25705 From Positions: 304 To 332

2
1
0
1












Swiss-Prot Disease: VAR_069769
p.ARG329CYS
N/A
N/A
Mitochondrial complex V deficiency, nuclear 4 (MC5DN4)


OMIM Disease: 164360.0001
p.ARG329CYS
N/A
N/A
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4||(1 family)






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