A mutation in NRL is associated with autosomal dominant retinitis pigmentosa

Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/40404

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Campo DC	Valor	Lengua/Idioma
dc.contributor.author	Bessant, David A. R.	-
dc.contributor.author	Bhattacharya, Shom Shanker	-
dc.date.accessioned	2011-09-30T12:09:44Z	-
dc.date.available	2011-09-30T12:09:44Z	-
dc.date.issued	1999	-
dc.identifier.citation	Nature Genetics 21: 355-356 (1999)	es_ES
dc.identifier.issn	1061-4036	-
dc.identifier.uri	http://hdl.handle.net/10261/40404	-
dc.description	2 páginas, 2 figuras.-- et al.	es_ES
dc.description.sponsorship	D.A.R.B. and A.M.P. are supported by the Medical Research Council of the U.K. (grant no. G9301094) and Q.-L.W. is a recipient of a Knights Templar Foundation fellowship. This research was supported by grants from the National Institutes of Health (EY11115, EY09769).	es_ES
dc.language.iso	eng	es_ES
dc.publisher	Nature Publishing Group	es_ES
dc.rights	closedAccess	es_ES
dc.title	A mutation in NRL is associated with autosomal dominant retinitis pigmentosa	es_ES
dc.type	artículo	es_ES
dc.identifier.doi	10.1038/7678	-
dc.description.peerreviewed	Peer reviewed	es_ES
dc.relation.publisherversion	http://dx.doi.org/10.1038/7678	es_ES
dc.identifier.e-issn	1546-1718	-
dc.type.coar	http://purl.org/coar/resource_type/c_6501	es_ES
item.openairetype	artículo	-
item.grantfulltext	none	-
item.cerifentitytype	Publications	-
item.openairecristype	http://purl.org/coar/resource_type/c_18cf	-
item.fulltext	No Fulltext	-
item.languageiso639-1	en	-
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