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Mutations on the Protein: Q7L5A8 From Positions: 19 To 37

2
1
0
1



Swiss-Prot Disease: VAR_054893
p.ASP35TYR
N/A
N/A
Spastic paraplegia 35, autosomal recessive (SPG35)


OMIM Disease: 611026.0002
p.ASP35TYR
N/A
N/A
SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE






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