peroxisome biogenesis factor 13, isoform CRA_d [Homo sapiens]

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Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. [Orphanet J Rare Dis. 2022]
Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders.
Borgia P, Baldassari S, Pedemonte N, Alkhunaizi E, D'Onofrio G, Tortora D, Calì E, Scudieri P, Balagura G, Musante I, et al. Orphanet J Rare Dis. 2022 Jul 19; 17(1):286. Epub 2022 Jul 19.
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis. [Hum Mol Genet. 2013]
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.
Krause C, Rosewich H, Woehler A, Gärtner J. Hum Mol Genet. 2013 Oct 1; 22(19):3844-57. Epub 2013 May 27.
Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. [Am J Med Genet A. 2009]
Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations.
Al-Dirbashi OY, Shaheen R, Al-Sayed M, Al-Dosari M, Makhseed N, Abu Safieh L, Santa T, Meyer BF, Shimozawa N, Alkuraya FS. Am J Med Genet A. 2009 Jun; 149A(6):1219-23.

RefSeq genomic sequence
See the genomic reference sequence for the PEX13 gene (NG_008665.1).
RefSeq protein
See the reference protein sequence for peroxisome biogenesis factor 13 (NP_002609.1).

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Protein