Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

Source:http://linkedlifedata.com/resource/pubmed/id/10051604

Proc. Natl. Acad. Sci. U.S.A. 1999 Mar 2 96 5 2116-21

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PMID
10051604