NIPA1: Difference between revisions
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'''Non-imprinted in Prader-Willi/Angelman syndrome region protein 1''' is a [[protein]] that in humans is encoded by the ''NIPA1'' [[gene]].<ref name="pmid14508710">{{cite journal | author = Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK | title = NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6) | journal = Am J Hum Genet | volume = 73 | issue = 4 | pages = |
'''Non-imprinted in Prader-Willi/Angelman syndrome region protein 1''' is a [[protein]] that in humans is encoded by the ''NIPA1'' [[gene]].<ref name="pmid14508710">{{cite journal | author = Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK | title = NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6) | journal = Am J Hum Genet | volume = 73 | issue = 4 | pages = 967–71 | year = 2003 | month = Sep | pmid = 14508710 | pmc = 1180617 | doi = 10.1086/378817 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=123606| accessdate = }}</ref> |
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Revision as of 20:44, 15 April 2010
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
- ^ 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) - ^ "Entrez Gene: NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1".
Further reading
 | This article on a gene on human chromosome 15 is a stub. You can help Wikipedia by expanding it. |