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Q34380791-382B9E97-1EC5-4AB6-89D0-FA49D5C1618A
Q34380791-382B9E97-1EC5-4AB6-89D0-FA49D5C1618A
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Statement
http://www.wikidata.org/entity/statement/Q34380791-382B9E97-1EC5-4AB6-89D0-FA49D5C1618A
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population
P2860
Q34380791-382B9E97-1EC5-4AB6-89D0-FA49D5C1618A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34380791-382B9E97-1EC5-4AB6-89D0-FA49D5C1618A
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wasDerivedFrom
91f4ea624590a9e37ede7862c2023d0e54cb1ff4
P2860
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum