Molecular characterization of G6PD deficiency by natural and amplification created restriction sites - Five mutations account for most G6PD deficiency cases in Taiwan

Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/22123

Title:	Molecular characterization of G6PD deficiency by natural and amplification created restriction sites - Five mutations account for most G6PD deficiency cases in Taiwan
Authors:	Chang, J-G. Chiou, S-S. Perng, L-I. Chen, T-C. Liu, T-C. Lee, L-S. Chen, P-H. Tang, T. K.
Issue Date:	1992
Relation:	Blood 80, 1079-1082
URI:	http://ir.sinica.edu.tw/handle/201000000A/22123
ISSN:	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0006-4971&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL:	http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=1323345
Appears in Collections:	生物醫學科學研究所

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