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1
S10038-007-0157-Y
S10038-007-0157-Y
http://dx.doi.org/10.1007/S10038-007-0157-Y
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C
P356
Q24307402-FD3A968B-B188-4BAE-84FD-7E8EBCC1AB0A
P356
S10038-007-0157-Y
http://dx.doi.org/10.1007/S10038-007-0157-Y