NIPA1

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Template:PBB Non-imprinted in Prader-Willi/Angelman syndrome region protein 1 is a protein that in humans is encoded by the NIPA1 gene.[1][2] Template:PBB Summary

References

  1. ^ Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK (2003). "NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6)". Am J Hum Genet. 73 (4): 967–71. doi:10.1086/378817. PMC 1180617. PMID 14508710. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  2. ^ "Entrez Gene: NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1".

Further reading

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