ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Prader–Willi syndrome (PWS) is associated with paternal gene deficiencies in human chromosome 15q11–13, suggesting that PWS is caused by a deficiency in one or more maternally imprinted genes. We have now mapped a gene, Snrpn, encoding a brain–enriched small nuclear ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng1292-259
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