PubMed (OMIM) for id: 766874

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Year	Number of Results
1998	1
1999	1
2002	2
2023	0

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The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.

Honsho M, Hiroshige T, Fujiki Y. Honsho M, et al. J Biol Chem. 2002 Nov 15;277(46):44513-24. doi: 10.1074/jbc.M206139200. Epub 2002 Sep 9. J Biol Chem. 2002. PMID: 12223482 Free article.

A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.

Shimozawa N, Nagase T, Takemoto Y, Suzuki Y, Fujiki Y, Wanders RJ, Kondo N. Shimozawa N, et al. Biochem Biophys Res Commun. 2002 Mar 22;292(1):109-12. doi: 10.1006/bbrc.2002.6642. Biochem Biophys Res Commun. 2002. PMID: 11890679

Peroxisome synthesis in the absence of preexisting peroxisomes.

South ST, Gould SJ. South ST, et al. J Cell Biol. 1999 Jan 25;144(2):255-66. doi: 10.1083/jcb.144.2.255. J Cell Biol. 1999. PMID: 9922452 Free PMC article.

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Honsho M, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. Honsho M, et al. Am J Hum Genet. 1998 Dec;63(6):1622-30. doi: 10.1086/302161. Am J Hum Genet. 1998. PMID: 9837814 Free PMC article.

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