Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice.
Data(s) |
01/01/2002
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Identificador |
http://dx.doi.org/10.1093/hmg/11.5.547 http://www.scopus.com/inward/record.url?scp=0036501462&partnerID=8YFLogxK |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Kennan , A , Aherne , A , Palfi , A , Humphries , M , McKee , A , Stitt , A , Simpson , D , Demtroder , K , Orntoft , T , Ayuso , C , Kenna , P F , Farrar , G J & Humphries , P 2002 , ' Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho-/- mice. ' Human Molecular Genetics , vol 11(5) , no. 5 , pp. 547-558 . DOI: 10.1093/hmg/11.5.547 |
Palavras-Chave | #/dk/atira/pure/subjectarea/asjc/1300/1311 #Genetics |
Tipo |
article |