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Mutations on the Protein: P13498 From Positions: 156 To 166

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1
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Swiss-Prot Disease: VAR_005126
p.PRO156GLN
N/A
N/A
Granulomatous disease, chronic, cytochrome-b-negative, autosomal recessive (ARCGD)


OMIM Disease: 608508.0005
p.PRO156GLN
N/A
N/A
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE






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