Molecular Basis of the Kell-null Phenotype: A Mutation at the Splice Site of Human KEL Gene Abolishes the Expression of Kell Blood Group Antigens

Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/8042

Title:	Molecular Basis of the Kell-null Phenotype: A Mutation at the Splice Site of Human KEL Gene Abolishes the Expression of Kell Blood Group Antigens
Authors:	Yu, L C Twu, Y C Chang, C Y Lin, M
Issue Date:	2001
Relation:	J Biol Chem 276, 10247-10252
URI:	http://ir.sinica.edu.tw/handle/201000000A/8042
ISSN:	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0021-9258&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL:	http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11134029
Appears in Collections:	生物化學研究所

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