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Q42291746-8EAC85AF-F1C5-41DF-A39F-58A954A0FDCC
Q42291746-8EAC85AF-F1C5-41DF-A39F-58A954A0FDCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-8EAC85AF-F1C5-41DF-A39F-58A954A0FDCC
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
P2860
Q42291746-8EAC85AF-F1C5-41DF-A39F-58A954A0FDCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-8EAC85AF-F1C5-41DF-A39F-58A954A0FDCC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
ec4207bc955d55300fb3cb5eee84a443b28ec621
P2860
[Hereditary peroxisomal diseases].