Publication: Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region
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Özçelik, T., Leff, S., Robinson, W., Donlon, T., Lalande, M., Sanjines, E., Schinzel, A., & Francke, U. (1992). Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region. Nature Genetics, 2, 265–269. https://doi.org/10.1038/ng1292-265
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Abstract
Prader–Willi syndrome (PWS) is associated with paternally derived chromosomal deletions in region 15q11–13 or with maternal disomy for chromosome 15. Therefore, loss of the expressed paternal alleles of maternally imprinted genes must be responsible for the PWS phenotype. We have mapped the gene encoding the small nuclear RNA associated polypeptide SmN (SNRPN) to human chromosome 15q12 and a processed pseudogene SNRPNP1 to chromosome region 6pter–p21. Furthermore, SNRPN was mapped to the minimal deletion interval that is critical for
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- Özçelik, Tayfun
- Leff, Stuart
- Robinson, Wendy
- Donlon, Tim
- Lalande, Marc
- Sanjines, Elvira
- Schinzel, Albert
- Francke, Uta
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Özçelik, T., Leff, S., Robinson, W., Donlon, T., Lalande, M., Sanjines, E., Schinzel, A., & Francke, U. (1992). Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region. Nature Genetics, 2, 265–269. https://doi.org/10.1038/ng1292-265
