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Q34380791-7D5D5A16-E124-4F1F-9039-67E9AA86E25C
Q34380791-7D5D5A16-E124-4F1F-9039-67E9AA86E25C
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Statement
http://www.wikidata.org/entity/statement/Q34380791-7D5D5A16-E124-4F1F-9039-67E9AA86E25C
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population
P2860
Q34380791-7D5D5A16-E124-4F1F-9039-67E9AA86E25C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34380791-7D5D5A16-E124-4F1F-9039-67E9AA86E25C
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wasDerivedFrom
91f4ea624590a9e37ede7862c2023d0e54cb1ff4
P2860
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders