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0e3b51fb1d5218181d88da5dcfcf173119f39fd0
0e3b51fb1d5218181d88da5dcfcf173119f39fd0
Reference
http://www.wikidata.org/reference/0e3b51fb1d5218181d88da5dcfcf173119f39fd0
Q189167-19FDB449-BBB3-4BAB-9F25-197D41254696
wasDerivedFrom
0e3b51fb1d5218181d88da5dcfcf173119f39fd0
Reference
http://www.wikidata.org/reference/0e3b51fb1d5218181d88da5dcfcf173119f39fd0
type
Reference
P248
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G