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Q34380791-BEF91B8F-960E-49BB-8820-B5BC487C8558
Q34380791-BEF91B8F-960E-49BB-8820-B5BC487C8558
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Statement
http://www.wikidata.org/entity/statement/Q34380791-BEF91B8F-960E-49BB-8820-B5BC487C8558
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population
P2860
Q34380791-BEF91B8F-960E-49BB-8820-B5BC487C8558
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34380791-BEF91B8F-960E-49BB-8820-B5BC487C8558
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wasDerivedFrom
91f4ea624590a9e37ede7862c2023d0e54cb1ff4
P2860
Occurrence of cerebrohepatorenal (Zellweger) syndrome in the Karaite community in Israel: a genetic hypothesis.