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Items: 3

1.
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.
Y Liu, J Björkman, A Urquhart, R J Wanders, D I Crane, S J Gould
Am J Hum Genet. 1999 Sep; 65(3): 621–634. doi: 10.1086/302534
PMCID:
PMC1377968
SummaryPDF–1.0M
2.
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
M Honsho, S Tamura, N Shimozawa, Y Suzuki, N Kondo, Y Fujiki
Am J Hum Genet. 1998 Dec; 63(6): 1622–1630. doi: 10.1086/302161
PMCID:
PMC1377633
SummaryPDF–1.2M
3.
PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G
Kamran Ghaedi, Masanori Honsho, Nobuyuki Shimozawa, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki
Am J Hum Genet. 2000 Oct; 67(4): 976–981. Published online 2000 Aug 31. doi: 10.1086/303086
PMCID:
PMC1287899
AbstractArticlePDF–585K

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