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Q24307402-78BB8322-68E4-4D9E-A09A-2121746BCB7F
Q24307402-78BB8322-68E4-4D9E-A09A-2121746BCB7F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307402-78BB8322-68E4-4D9E-A09A-2121746BCB7F
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
P31
Q24307402-78BB8322-68E4-4D9E-A09A-2121746BCB7F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307402-78BB8322-68E4-4D9E-A09A-2121746BCB7F
rank
NormalRank
type
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Statement
P31
scholarly article