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Q24540126-FEA518F0-1064-42F1-A3FA-BA2243AB8EAD
Q24540126-FEA518F0-1064-42F1-A3FA-BA2243AB8EAD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24540126-FEA518F0-1064-42F1-A3FA-BA2243AB8EAD
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.
P2860
Q24540126-FEA518F0-1064-42F1-A3FA-BA2243AB8EAD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24540126-FEA518F0-1064-42F1-A3FA-BA2243AB8EAD
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Statement
wasDerivedFrom
8a798c1f9c78b490490d39a01d7cf8b7401cc2f9
P2860
Identification of a common PEX1 mutation in Zellweger syndrome