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Maternal imprinting of human SNRPN, a gene deleted in Prader–Willi syndrome

✍ Scribed by Reed, Martha L.; Leff, Stuart E.


Book ID
109915144
Publisher
Nature Publishing Group
Year
1994
Tongue
English
Weight
640 KB
Volume
6
Category
Article
ISSN
1061-4036

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## Abstract Prader–Willi syndrome (PWS) is caused by loss of paternally expressed genes in the 15q11‐q13 region. To further characterize alterations in gene expression in this classical obesity syndrome we used whole genome microarrays to study a PWS mouse model resulting from a paternally derived