-
1
-
-
84883573937
-
Genetic cardiomyopathies causing heart failure
-
Cahill TJ, Ashrafian H, Watkins H. Genetic cardiomyopathies causing heart failure. Circ Res. 2013;113:660-675.
-
(2013)
Circ Res.
, vol.113
, pp. 660-675
-
-
Cahill, T.J.1
Ashrafian, H.2
Watkins, H.3
-
2
-
-
77957267604
-
The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease
-
Delmar M, McKenna WJ. The cardiac desmosome and arrhythmogenic cardiomyopathies: from gene to disease. Circ Res. 2010;107:700-714.
-
(2010)
Circ Res.
, vol.107
, pp. 700-714
-
-
Delmar, M.1
McKenna, W.J.2
-
3
-
-
0022630109
-
Fractionation of membrane proteins by temperature-induced phase separation in Triton X-114. Application to subcellular fractions of the adrenal medulla
-
Pryde JG, Phillips JH. Fractionation of membrane proteins by temperature-induced phase separation in Triton X-114. Application to subcellular fractions of the adrenal medulla. Biochem J. 1986;233:525-533.
-
(1986)
Biochem J.
, vol.233
, pp. 525-533
-
-
Pryde, J.G.1
Phillips, J.H.2
-
4
-
-
79952764520
-
Performance of mutation pathogenicity prediction methods on missense variants
-
Thusberg J, Olatubosun A, Vihinen M. Performance of mutation pathogenicity prediction methods on missense variants. Hum Mutat. 2011;32:358-368.
-
(2011)
Hum Mutat.
, vol.32
, pp. 358-368
-
-
Thusberg, J.1
Olatubosun, A.2
Vihinen, M.3
-
5
-
-
84893690123
-
Genetics of sudden cardiac death caused by ventricular arrhythmias
-
Marsman RF, Tan HL, Bezzina CR. Genetics of sudden cardiac death caused by ventricular arrhythmias. Nat Rev Cardiol. 2014;11:96-111.
-
(2014)
Nat Rev Cardiol.
, vol.11
, pp. 96-111
-
-
Marsman, R.F.1
Tan, H.L.2
Bezzina, C.R.3
-
6
-
-
79956116043
-
SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism
-
McNair WP, Sinagra G, Taylor MR, Di Lenarda A, Ferguson DA, Salcedo EE, Slavov D, Zhu X, Caldwell JH, Mestroni L. SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. J Am Coll Cardiol. 2011;57:2160-2168.
-
(2011)
J Am Coll Cardiol.
, vol.57
, pp. 2160-2168
-
-
McNair, W.P.1
Sinagra, G.2
Taylor, M.R.3
Di Lenarda, A.4
Ferguson, D.A.5
Salcedo, E.E.6
Slavov, D.7
Zhu, X.8
Caldwell, J.H.9
Mestroni, L.10
-
7
-
-
5644229494
-
SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia
-
McNair WP, Ku L, Taylor MR, Fain PR, Dao D, Wolfel E, Mestroni L. SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. Circulation. 2004;110:2163-2167.
-
(2004)
Circulation.
, vol.110
, pp. 2163-2167
-
-
McNair, W.P.1
Ku, L.2
Taylor, M.R.3
Fain, P.R.4
Dao, D.5
Wolfel, E.6
Mestroni, L.7
-
8
-
-
12144290256
-
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating
-
Bienengraeber M, Olson TM, Selivanov VA, Kathmann EC, O'Cochlain F, Gao F, Karger AB, Ballew JD, Hodgson DM, Zingman LV, Pang YP, Alekseev AE, Terzic A. ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. Nat Genet. 2004;36:382-387.
-
(2004)
Nat Genet.
, vol.36
, pp. 382-387
-
-
Bienengraeber, M.1
Olson, T.M.2
Selivanov, V.A.3
Kathmann, E.C.4
O'Cochlain, F.5
Gao, F.6
Karger, A.B.7
Ballew, J.D.8
Hodgson, D.M.9
Zingman, L.V.10
Pang, Y.P.11
Alekseev, A.E.12
Terzic, A.13
-
9
-
-
84863000739
-
Dominant missense mutations in ABCC9 cause Cantu syndrome
-
Harakalova M, van Harssel JJ, Terhal PA, van Lieshout S, Duran K, Renkens I, Amor DJ, Wilson LC, Kirk EP, Turner CL, Shears D, Garcia-Minaur S, Lees MM, Ross A, Venselaar H, Vriend G, Takanari H, Rook MB, van der Heyden MA, Asselbergs FW, Breur HM, Swinkels ME, Scurr IJ, Smithson SF, Knoers NV, van der Smagt JJ, Nijman IJ, Kloosterman WP, van Haelst MM, van Haaften G, Cuppen E. Dominant missense mutations in ABCC9 cause Cantu syndrome. Nat Genet. 2012;44:793-796.
-
(2012)
Nat Genet.
, vol.44
, pp. 793-796
-
-
Harakalova, M.1
van Harssel, J.J.2
Terhal, P.A.3
van Lieshout, S.4
Duran, K.5
Renkens, I.6
Amor, D.J.7
Wilson, L.C.8
Kirk, E.P.9
Turner, C.L.10
Shears, D.11
Garcia-Minaur, S.12
Lees, M.M.13
Ross, A.14
Venselaar, H.15
Vriend, G.16
Takanari, H.17
Rook, M.B.18
van der Heyden, M.A.19
Asselbergs, F.W.20
Breur, H.M.21
Swinkels, M.E.22
Scurr, I.J.23
Smithson, S.F.24
Knoers, N.V.25
van der Smagt, J.J.26
Nijman, I.J.27
Kloosterman, W.P.28
van Haelst, M.M.29
van Haaften, G.30
Cuppen, E.31
more..
-
10
-
-
84862778065
-
Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
-
Barajas-Martinez H, Hu D, Ferrer T, Onetti CG, Wu Y, Burashnikov E, Boyle M, Surman T, Urrutia J, Veltmann C, Schimpf R, Borggrefe M, Wolpert C, Ibrahim BB, Sanchez-Chapula JA, Winters S, Haissaguerre M, Antzelevitch C. Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8. Heart Rhythm. 2012;9:548-555.
-
(2012)
Heart Rhythm.
, vol.9
, pp. 548-555
-
-
Barajas-Martinez, H.1
Hu, D.2
Ferrer, T.3
Onetti, C.G.4
Wu, Y.5
Burashnikov, E.6
Boyle, M.7
Surman, T.8
Urrutia, J.9
Veltmann, C.10
Schimpf, R.11
Borggrefe, M.12
Wolpert, C.13
Ibrahim, B.B.14
Sanchez-Chapula, J.A.15
Winters, S.16
Haissaguerre, M.17
Antzelevitch, C.18
-
11
-
-
0345861903
-
Electrophysiological changes in heart failure and their relationship to arrhythmogenesis
-
Janse MJ. Electrophysiological changes in heart failure and their relationship to arrhythmogenesis. Cardiovasc Res. 2004;61:208-217.
-
(2004)
Cardiovasc Res.
, vol.61
, pp. 208-217
-
-
Janse, M.J.1
-
12
-
-
84907048399
-
Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP(2)
-
Dvir M, Strulovich R, Sachyani D, Ben-Tal Cohen I, Haitin Y, Dessauer C, Pongs O, Kass R, Hirsch JA, Attali B. Long QT mutations at the interface between KCNQ1 helix C and KCNE1 disrupt I(KS) regulation by PKA and PIP(2). J Cell Sci. 2014;127:3943-3955.
-
(2014)
J Cell Sci.
, vol.127
, pp. 3943-3955
-
-
Dvir, M.1
Strulovich, R.2
Sachyani, D.3
Ben-Tal Cohen, I.4
Haitin, Y.5
Dessauer, C.6
Pongs, O.7
Kass, R.8
Hirsch, J.A.9
Attali, B.10
-
13
-
-
84894535231
-
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation
-
Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP. A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation. Heart Rhythm. 2014;11:459-468.
-
(2014)
Heart Rhythm.
, vol.11
, pp. 459-468
-
-
Bartos, D.C.1
Giudicessi, J.R.2
Tester, D.J.3
Ackerman, M.J.4
Ohno, S.5
Horie, M.6
Gollob, M.H.7
Burgess, D.E.8
Delisle, B.P.9
-
14
-
-
4644368376
-
Overexpression of beta2-adrenergic receptors cAMP-dependent protein kinase phosphorylates and modulates slow delayed rectifier potassium channels expressed in murine heart: evidence for receptor/channel co-localization
-
Dilly KW, Kurokawa J, Terrenoire C, Reiken S, Lederer WJ, Marks AR, Kass RS. Overexpression of beta2-adrenergic receptors cAMP-dependent protein kinase phosphorylates and modulates slow delayed rectifier potassium channels expressed in murine heart: evidence for receptor/channel co-localization. J Biol Chem. 2004;279:40778-40787.
-
(2004)
J Biol Chem.
, vol.279
, pp. 40778-40787
-
-
Dilly, K.W.1
Kurokawa, J.2
Terrenoire, C.3
Reiken, S.4
Lederer, W.J.5
Marks, A.R.6
Kass, R.S.7
-
16
-
-
33646814436
-
KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin
-
Ghosh S, Nunziato DA, Pitt GS. KCNQ1 assembly and function is blocked by long-QT syndrome mutations that disrupt interaction with calmodulin. Circ Res. 2006;98:1048-1054.
-
(2006)
Circ Res.
, vol.98
, pp. 1048-1054
-
-
Ghosh, S.1
Nunziato, D.A.2
Pitt, G.S.3
-
17
-
-
84897056371
-
Exchange protein directly activated by cAMP mediates slow delayed-rectifier current remodeling by sustained beta-adrenergic activation in guinea pig hearts
-
Aflaki M, Qi XY, Xiao L, Ordog B, Tadevosyan A, Luo X, Maguy A, Shi Y, Tardif JC, Nattel S. Exchange protein directly activated by cAMP mediates slow delayed-rectifier current remodeling by sustained beta-adrenergic activation in guinea pig hearts. Circ Res. 2014;114:993-1003.
-
(2014)
Circ Res.
, vol.114
, pp. 993-1003
-
-
Aflaki, M.1
Qi, X.Y.2
Xiao, L.3
Ordog, B.4
Tadevosyan, A.5
Luo, X.6
Maguy, A.7
Shi, Y.8
Tardif, J.C.9
Nattel, S.10
-
18
-
-
84857064601
-
Attenuated ventricular beta-adrenergic response and reduced repolarization reserve in a rabbit model of chronic heart failure
-
Nissen JD, Thomsen MB, Bentzen BH, Diness JG, Diness TG, Jespersen T, Grunnet M. Attenuated ventricular beta-adrenergic response and reduced repolarization reserve in a rabbit model of chronic heart failure. J Cardiovasc Pharmacol. 2012;59:142-150.
-
(2012)
J Cardiovasc Pharmacol.
, vol.59
, pp. 142-150
-
-
Nissen, J.D.1
Thomsen, M.B.2
Bentzen, B.H.3
Diness, J.G.4
Diness, T.G.5
Jespersen, T.6
Grunnet, M.7
-
19
-
-
33646053171
-
Tumor necrosis factor-alpha inhibits the cardiac delayed rectifier K current via the asphingomyelin pathway
-
Hatada K, Washizuka T, Horie M, Watanabe H, Yamashita F, Chinushi M, Aizawa Y. Tumor necrosis factor-alpha inhibits the cardiac delayed rectifier K current via the asphingomyelin pathway. Biochem Biophys Res Commun. 2006;344:189-193.
-
(2006)
Biochem Biophys Res Commun.
, vol.344
, pp. 189-193
-
-
Hatada, K.1
Washizuka, T.2
Horie, M.3
Watanabe, H.4
Yamashita, F.5
Chinushi, M.6
Aizawa, Y.7
-
20
-
-
84856058439
-
Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1
-
Heijman J, Spatjens RL, Seyen SR, Lentink V, Kuijpers HJ, Boulet IR, de Windt LJ, David M, Volders PG. Dominant-negative control of cAMP-dependent IKs upregulation in human long-QT syndrome type 1. Circ Res. 2012;110:211-219.
-
(2012)
Circ Res.
, vol.110
, pp. 211-219
-
-
Heijman, J.1
Spatjens, R.L.2
Seyen, S.R.3
Lentink, V.4
Kuijpers, H.J.5
Boulet, I.R.6
de Windt, L.J.7
David, M.8
Volders, P.G.9
-
21
-
-
34447567309
-
Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity
-
Yeung SY, Pucovsky V, Moffatt JD, Saldanha L, Schwake M, Ohya S, Greenwood IA. Molecular expression and pharmacological identification of a role for K(v)7 channels in murine vascular reactivity. Br J Pharmacol. 2007;151:758-770.
-
(2007)
Br J Pharmacol.
, vol.151
, pp. 758-770
-
-
Yeung, S.Y.1
Pucovsky, V.2
Moffatt, J.D.3
Saldanha, L.4
Schwake, M.5
Ohya, S.6
Greenwood, I.A.7
-
22
-
-
84888101953
-
Intracellular ATP binding is required to activate the slowly activating K+ channel I(Ks)
-
Li Y, Gao J, Lu Z, McFarland K, Shi J, Bock K, Cohen IS, Cui J. Intracellular ATP binding is required to activate the slowly activating K+ channel I(Ks). Proc Natl Acad Sci USA. 2013;110:18922-18927.
-
(2013)
Proc Natl Acad Sci USA.
, vol.110
, pp. 18922-18927
-
-
Li, Y.1
Gao, J.2
Lu, Z.3
McFarland, K.4
Shi, J.5
Bock, K.6
Cohen, I.S.7
Cui, J.8
-
23
-
-
84902682885
-
Mechano-electrical coupling as framework for understanding functional remodeling during LBBB and CRT
-
Kuijpers NH, Hermeling E, Lumens J, ten Eikelder HM, Delhaas T, Prinzen FW. Mechano-electrical coupling as framework for understanding functional remodeling during LBBB and CRT. Am J Physiol Heart Circ Physiol. 2014;306:H1644-H1659.
-
(2014)
Am J Physiol Heart Circ Physiol.
, vol.306
, pp. H1644-H1659
-
-
Kuijpers, N.H.1
Hermeling, E.2
Lumens, J.3
ten Eikelder, H.M.4
Delhaas, T.5
Prinzen, F.W.6
-
24
-
-
84883589824
-
Electromechanical dyssynchrony and resynchronization of the failing heart
-
Kirk JA, Kass DA. Electromechanical dyssynchrony and resynchronization of the failing heart. Circ Res. 2013;113:765-776.
-
(2013)
Circ Res.
, vol.113
, pp. 765-776
-
-
Kirk, J.A.1
Kass, D.A.2
-
25
-
-
84883163817
-
Dilated cardiomyopathy: the complexity of a diverse genetic architecture
-
Hershberger RE, Hedges DJ, Morales A. Dilated cardiomyopathy: the complexity of a diverse genetic architecture. Nat Rev Cardiol. 2013;10:531-547.
-
(2013)
Nat Rev Cardiol.
, vol.10
, pp. 531-547
-
-
Hershberger, R.E.1
Hedges, D.J.2
Morales, A.3
-
26
-
-
84892387550
-
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy
-
Rigato I, Bauce B, Rampazzo A, Zorzi A, Pilichou K, Mazzotti E, Migliore F, Marra MP, Lorenzon A, De Bortoli M, Calore M, Nava A, Daliento L, Gregori D, Iliceto S, Thiene G, Basso C, Corrado D. Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy. Circ Cardiovasc Genet. 2013;6:533-542.
-
(2013)
Circ Cardiovasc Genet.
, vol.6
, pp. 533-542
-
-
Rigato, I.1
Bauce, B.2
Rampazzo, A.3
Zorzi, A.4
Pilichou, K.5
Mazzotti, E.6
Migliore, F.7
Marra, M.P.8
Lorenzon, A.9
De Bortoli, M.10
Calore, M.11
Nava, A.12
Daliento, L.13
Gregori, D.14
Iliceto, S.15
Thiene, G.16
Basso, C.17
Corrado, D.18
-
27
-
-
77449112270
-
Nature's genetic gradients and the clinical phenotype
-
Marian AJ. Nature's genetic gradients and the clinical phenotype. Circ Cardiovasc Genet. 2009;2:537-539.
-
(2009)
Circ Cardiovasc Genet.
, vol.2
, pp. 537-539
-
-
Marian, A.J.1
-
28
-
-
0037428218
-
KCNQ1 gain-of-function mutation in familial atrial fibrillation
-
Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB, Liu Y, Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J, Huang W. KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science. 2003;299:251-254.
-
(2003)
Science.
, vol.299
, pp. 251-254
-
-
Chen, Y.H.1
Xu, S.J.2
Bendahhou, S.3
Wang, X.L.4
Wang, Y.5
Xu, W.Y.6
Jin, H.W.7
Sun, H.8
Su, X.Y.9
Zhuang, Q.N.10
Yang, Y.Q.11
Li, Y.B.12
Liu, Y.13
Xu, H.J.14
Li, X.F.15
Ma, N.16
Mou, C.P.17
Chen, Z.18
Barhanin, J.19
Huang, W.20
more..
-
29
-
-
0029952101
-
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
-
Barhanin J, Lesage F, Guillemare E, Fink M, Lazdunski M, Romey G. K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current. Nature. 1996;384:78-80.
-
(1996)
Nature.
, vol.384
, pp. 78-80
-
-
Barhanin, J.1
Lesage, F.2
Guillemare, E.3
Fink, M.4
Lazdunski, M.5
Romey, G.6
-
30
-
-
2542491002
-
Mutation in the KCNQ1 gene leading to the short QT-interval syndrome
-
Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baro I, Wilde AA. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome. Circulation. 2004;109:2394-2397.
-
(2004)
Circulation.
, vol.109
, pp. 2394-2397
-
-
Bellocq, C.1
van Ginneken, A.C.2
Bezzina, C.R.3
Alders, M.4
Escande, D.5
Mannens, M.M.6
Baro, I.7
Wilde, A.A.8
-
31
-
-
84876933197
-
A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation
-
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. J Cardiovasc Electrophysiol. 2013;24:562-569.
-
(2013)
J Cardiovasc Electrophysiol.
, vol.24
, pp. 562-569
-
-
Bartos, D.C.1
Anderson, J.B.2
Bastiaenen, R.3
Johnson, J.N.4
Gollob, M.H.5
Tester, D.J.6
Burgess, D.E.7
Homfray, T.8
Behr, E.R.9
Ackerman, M.J.10
Guicheney, P.11
Delisle, B.P.12
-
32
-
-
67650738504
-
Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation
-
Das S, Makino S, Melman YF, Shea MA, Goyal SB, Rosenzweig A, Macrae CA, Ellinor PT. Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation. Heart Rhythm. 2009;6:1146-1153.
-
(2009)
Heart Rhythm.
, vol.6
, pp. 1146-1153
-
-
Das, S.1
Makino, S.2
Melman, Y.F.3
Shea, M.A.4
Goyal, S.B.5
Rosenzweig, A.6
Macrae, C.A.7
Ellinor, P.T.8
-
33
-
-
0034141999
-
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
-
Schmitt N, Schwarz M, Peretz A, Abitbol I, Attali B, Pongs O. A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly. EMBO J. 2000;19:332-340.
-
(2000)
EMBO J.
, vol.19
, pp. 332-340
-
-
Schmitt, N.1
Schwarz, M.2
Peretz, A.3
Abitbol, I.4
Attali, B.5
Pongs, O.6
-
34
-
-
84891519746
-
Recent molecular insights from mutated IKS channels in cardiac arrhythmia
-
Dvir M, Peretz A, Haitin Y, Attali B. Recent molecular insights from mutated IKS channels in cardiac arrhythmia. Curr Opin Pharmacol. 2014;15:74-82.
-
(2014)
Curr Opin Pharmacol.
, vol.15
, pp. 74-82
-
-
Dvir, M.1
Peretz, A.2
Haitin, Y.3
Attali, B.4
-
35
-
-
84896921083
-
Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young
-
Bagnall RD, Das KJ, Duflou J, Semsarian C. Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young. Heart Rhythm. 2014;11:655-662.
-
(2014)
Heart Rhythm.
, vol.11
, pp. 655-662
-
-
Bagnall, R.D.1
Das, K.J.2
Duflou, J.3
Semsarian, C.4
-
36
-
-
84872621095
-
A left ventricular noncompaction in a patient with long QT syndrome caused by a KCNQ1 mutation: a case report
-
Nakashima K, Kusakawa I, Yamamoto T, Hirabayashi S, Hosoya R, Shimizu W, Sumitomo N. A left ventricular noncompaction in a patient with long QT syndrome caused by a KCNQ1 mutation: a case report. Heart Vessels. 2013;28:126-129.
-
(2013)
Heart Vessels.
, vol.28
, pp. 126-129
-
-
Nakashima, K.1
Kusakawa, I.2
Yamamoto, T.3
Hirabayashi, S.4
Hosoya, R.5
Shimizu, W.6
Sumitomo, N.7
-
37
-
-
84890361301
-
DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies
-
D'Argenio V, Frisso G, Precone V, Boccia A, Fienga A, Pacileo G, Limongelli G, Paolella G, Calabro R, Salvatore F. DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies. J Mol Diagn. 2014;16:32-44.
-
(2014)
J Mol Diagn.
, vol.16
, pp. 32-44
-
-
D'Argenio, V.1
Frisso, G.2
Precone, V.3
Boccia, A.4
Fienga, A.5
Pacileo, G.6
Limongelli, G.7
Paolella, G.8
Calabro, R.9
Salvatore, F.10
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