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Article: Predicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studies

TitlePredicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studies
Authors
Li, MKwan, SHBao, SYang, WHo, SLSong, YSham, PC
Issue Date2013
PublisherPublic Library of Science. The Journal's web site is located at http://www.plosgenetics.org/
Citation
PLoS Genetics, 2013, v. 9 n. 1, article no. e1003143 How to Cite?
DOI: http://dx.doi.org/10.1371/journal.pgen.1003143
Persistent Identifierhttp://hdl.handle.net/10722/183690
ISI Accession Number ID
WOS:000314651500009

 

DC FieldValueLanguage
dc.contributor.authorLi, Men_US
dc.contributor.authorKwan, SHen_US
dc.contributor.authorBao, Sen_US
dc.contributor.authorYang, Wen_US
dc.contributor.authorHo, SLen_US
dc.contributor.authorSong, Yen_US
dc.contributor.authorSham, PCen_US
dc.date.accessioned2013-06-18T04:08:01Z-
dc.date.available2013-06-18T04:08:01Z-
dc.date.issued2013en_US
dc.identifier.citationPLoS Genetics, 2013, v. 9 n. 1, article no. e1003143en_US
dc.identifier.urihttp://hdl.handle.net/10722/183690-
dc.languageengen_US
dc.publisherPublic Library of Science. The Journal's web site is located at http://www.plosgenetics.org/-
dc.relation.ispartofPLoS Geneticsen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titlePredicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing Studiesen_US
dc.typeArticleen_US
dc.identifier.emailLi, M: mxli@hku.hken_US
dc.identifier.emailYang, W: yangwl@hkucc.hku.hken_US
dc.identifier.emailHo, SL: slho@hku.hken_US
dc.identifier.emailSong, Y: songy@hku.hken_US
dc.identifier.emailSham, PC: pcsham@hku.hken_US
dc.identifier.authorityLi, M=rp01722en_US
dc.identifier.authorityYang, W=rp00524en_US
dc.identifier.authorityHo, SL=rp00240en_US
dc.identifier.authoritySong, Y=rp00488en_US
dc.identifier.authoritySham, PC=rp00459en_US
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1371/journal.pgen.1003143-
dc.identifier.scopuseid_2-s2.0-84873486397-
dc.identifier.hkuros214862en_US
dc.identifier.hkuros239124-
dc.identifier.volume9en_US
dc.identifier.issue1en_US
dc.identifier.eissn1553-7404-
dc.identifier.isiWOS:000314651500009-
dc.identifier.issnl1553-7390-

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