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Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization.

AuthorsM Masuno, N Shimozawa, Y Suzuki, N Kondo, T Orii, T Tsukamoto, T Osumi, Y Fujiki, K Imaizumi, Y Kuroki
JournalGenomics (Genomics) Vol. 20 Issue 1 Pg. 141-2 (Mar 01 1994) ISSN: 0888-7543 [Print] United States
PMID8020947 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA, Complementary
  • Membrane Proteins
  • PEX2 protein, human
  • Peroxisomal Biogenesis Factor 2
Topics
  • Chromosome Mapping
  • Chromosomes, Human, Pair 8 (ultrastructure)
  • DNA, Complementary (genetics)
  • Genes, Recessive
  • Humans
  • In Situ Hybridization, Fluorescence
  • Membrane Proteins (genetics)
  • Peroxisomal Biogenesis Factor 2
  • Zellweger Syndrome (genetics)

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