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Official Full Name
necdin homolog (mouse)
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed;exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress;growth in postmitotic neurons.
NDN; necdin; Peg6; AI528698; necdin homolog (mouse); necdin (mouse) homolog; HsT16328; PWCR

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