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Q42291746-ED1F4D4A-7416-4B6C-A90E-3D7841F155E0
Q42291746-ED1F4D4A-7416-4B6C-A90E-3D7841F155E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-ED1F4D4A-7416-4B6C-A90E-3D7841F155E0
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
P2860
Q42291746-ED1F4D4A-7416-4B6C-A90E-3D7841F155E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-ED1F4D4A-7416-4B6C-A90E-3D7841F155E0
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Statement
wasDerivedFrom
ec4207bc955d55300fb3cb5eee84a443b28ec621
P2860
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6