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Dive into the research topics of 'A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population'. Together they form a unique fingerprint.- Sort by
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Sebastien Levesque, Charles Morin, Simon Pierre Guay, Josee Villeneuve, Pascale Marquis, Wing Y. Yik, Sarn Jiralerspong, Luigi Bouchard, Steven Steinberg, Joseph G. Hacia, Ken Dewar, Nancy E. Braverman
Research output: Contribution to journal › Article › peer-review