Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 Tri-snRNP integration and is associated with retinitis pigmentosa

Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0111754

DC Field	Value
dc.title	Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 Tri-snRNP integration and is associated with retinitis pigmentosa
dc.contributor.author	Linder B.
dc.contributor.author	Hirmer A.
dc.contributor.author	Gal A.
dc.contributor.author	R�ther K.
dc.contributor.author	Bolz H.J.
dc.contributor.author	Winkler C.
dc.contributor.author	Laggerbauer B.
dc.contributor.author	Fischer U.
dc.date.accessioned	2018-05-28T01:52:21Z
dc.date.available	2018-05-28T01:52:21Z
dc.date.issued	2014
dc.identifier.citation	Linder B., Hirmer A., Gal A., R�ther K., Bolz H.J., Winkler C., Laggerbauer B., Fischer U. (2014). Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 Tri-snRNP integration and is associated with retinitis pigmentosa. PLoS ONE 9 (11) : e111754. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0111754
dc.identifier.issn	19326203
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/142568
dc.publisher	Public Library of Science
dc.source	Scopus
dc.type	Article
dc.contributor.department	DEPT OF GEOGRAPHY
dc.description.doi	10.1371/journal.pone.0111754
dc.description.sourcetitle	PLoS ONE
dc.description.volume	9
dc.description.issue	11
dc.description.page	e111754
dc.identifier.isiut	000344816700020
dc.published.state	published
Appears in Collections:	Staff Publications Elements

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