Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus

Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus

Prader-Willi Syndrome (PWS) is a neurogenetic disorder caused by the deletion of imprinted genes on the paternally inherited human chromosome 15q11-q13. This locus harbours a long non-protein-coding RNA (U-UBE3A-ATS) that contains six intron-encoded snoRNAs, including the SNORD116 and SNORD115 repet...

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Bibliographic Details
Main Authors: Galiveti, Chenna R., Raabe, Carsten A., Konthur, Zoltán, Rozhdestvensky, Timofey S.
Format: Online
Language:English
Published: Nature Publishing Group 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171697/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171697/

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