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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.

The 70-kDa peroxisomal membrane protein (PXMP1) is a member of the ATP-binding cassette transporter family. In humans, mutations in this gene may be responsible for a subset of patients with Zellweger syndrome, a lethal inborn error of peroxisome assembly. The PXMP1 gene was assigned to human chromosome 1p21-p22 by in situ hybridization and its murine homologue ( Pxmp-1) to chromosome 3 by interspecific backcross analysis.[1]

References

  1. Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3. Gärtner, J., Kearns, W., Rosenberg, C., Pearson, P., Copeland, N.G., Gilbert, D.J., Jenkins, N.A., Valle, D. Genomics (1993) [Pubmed]
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