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Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/88678
Title: Rare coding variants in RCN3 are associated with blood pressure
Authors: He, KY
Kelly, TN
Wang, H
Liang, J
Zhu, L
Cade, BE
Assimes, TL
Becker, LC
Beitelshees, AL
Bielak, LF
Bress, AP
Brody, JA
Chang, YC
Chang, YC 
de Vries, PS
Duggirala, R
Fox, ER
Franceschini, N
Furniss, AL
Gao, Y
Guo, X
Haessler, J
Hung, YJ
Hwang, SJ
Irvin, MR
Kalyani, RR
Liu, CT
Liu, C
Martin, LW
Montasser, ME
Muntner, PM
Mwasongwe, S
Naseri, T
Palmas, W
Reupena, MS
Rice, KM
Sheu, WH
Shimbo, D
Smith, JA
Snively, BM
Yanek, LR
Zhao, W
Blangero, J
Boerwinkle, E
Chen, YI
Correa, A
Cupples, LA
Curran, JE
Fornage, M
He, J
Hou, L
Kaplan, RC
Kardia, SLR
Kenny, EE
Kooperberg, C
Lloyd-Jones, D
Loos, RJF
Mathias, RA
McGarvey, ST
Mitchell, BD
North, KE
Peyser, PA
Psaty, BM
Raffield, LM
Rao, DC
Redline, S
Reiner, AP
Rich, SS
Rotter, JI
Taylor, KD
Tracy, R
Vasan, RS
Morrison, AC
Levy, D
Chakravarti, A
Arnett, DK
Zhu, X
Issue Date: 2022
Relation: BMC genomics 23(1), 148
URI: http://ir.sinica.edu.tw/handle/201000000A/88678
ISSN: http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=1471-2164&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL: http://dx.doi.org/10.1186/s12864-022-08356-4
Appears in Collections:生物醫學科學研究所

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