-
1
-
-
80053385333
-
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
-
Kooner, J.S., Saleheen, D., Sim, X., Sehmi, J., Zhang, W., Frossard, P., Been, L.F., Chia, K.S., Dimas, A.S., Hassanali, N. et al. (2011) Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat. Genet., 43, 984-989.
-
(2011)
Nat. Genet.
, vol.43
, pp. 984-989
-
-
Kooner, J.S.1
Saleheen, D.2
Sim, X.3
Sehmi, J.4
Zhang, W.5
Frossard, P.6
Been, L.F.7
Chia, K.S.8
Dimas, A.S.9
Hassanali, N.10
-
2
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
Speliotes, E.K., Willer, C.J., Berndt, S.I., Monda, K.L., Thorleifsson, G., Jackson, A.U., Lango Allen, H., Lindgren, C.M., Luan, J., Magi, R. et al. (2010) Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat. Genet., 42, 937-948.
-
(2010)
Nat. Genet.
, vol.42
, pp. 937-948
-
-
Speliotes, E.K.1
Willer, C.J.2
Berndt, S.I.3
Monda, K.L.4
Thorleifsson, G.5
Jackson, A.U.6
Lango Allen, H.7
Lindgren, C.M.8
Luan, J.9
Magi, R.10
-
3
-
-
70749096913
-
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
-
Kathiresan, S., Voight, B.F., Purcell, S., Musunuru, K., Ardissino, D., Mannucci, P.M., Anand, S., Engert, J.C., Samani, N.J., Schunkert, H. et al. (2009) Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat. Genet., 41, 334-341.
-
(2009)
Nat. Genet.
, vol.41
, pp. 334-341
-
-
Kathiresan, S.1
Voight, B.F.2
Purcell, S.3
Musunuru, K.4
Ardissino, D.5
Mannucci, P.M.6
Anand, S.7
Engert, J.C.8
Samani, N.J.9
Schunkert, H.10
-
4
-
-
84947899509
-
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
-
Lu, Y., Vitart, V., Burdon, K.P., Khor, C.C., Bykhovskaya, Y., Mirshahi, A., Hewitt, A.W., Koehn, D., Hysi, P.G., Ramdas, W.D. et al. (2013) Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat. Genet., 45, 155-163.
-
(2013)
Nat. Genet.
, vol.45
, pp. 155-163
-
-
Lu, Y.1
Vitart, V.2
Burdon, K.P.3
Khor, C.C.4
Bykhovskaya, Y.5
Mirshahi, A.6
Hewitt, A.W.7
Koehn, D.8
Hysi, P.G.9
Ramdas, W.D.10
-
5
-
-
77954164213
-
A genome-wide association study of optic disc parameters
-
Ramdas, W.D., van Koolwijk, L.M., Ikram, M.K., Jansonius, N.M., de Jong, P.T., Bergen, A.A., Isaacs, A., Amin, N., Aulchenko, Y.S., Wolfs, R.C. et al. (2010) A genome-wide association study of optic disc parameters. PLoS. Genet., 6, e1000978.
-
(2010)
PLoS. Genet.
, vol.6
-
-
Ramdas, W.D.1
Van Koolwijk, L.M.2
Ikram, M.K.3
Jansonius, N.M.4
de Jong, P.T.5
Bergen, A.A.6
Isaacs, A.7
Amin, N.8
Aulchenko, Y.S.9
Wolfs, R.C.10
-
6
-
-
80052242121
-
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore
-
Han, S., Chen, P., Fan, Q., Khor, C.C., Sim, X., Tay, W.T., Ong, R.T., Suo, C., Goh, L.K., Lavanya, R. et al. (2011) Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore. Hum. Mol. Genet., 20, 3693-3698.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 3693-3698
-
-
Han, S.1
Chen, P.2
Fan, Q.3
Khor, C.C.4
Sim, X.5
Tay, W.T.6
Ong, R.T.7
Suo, C.8
Goh, L.K.9
Lavanya, R.10
-
7
-
-
84855281926
-
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism
-
Fan, Q., Zhou, X., Khor, C.C., Cheng, C.Y., Goh, L.K., Sim, X., Tay, W.T., Li, Y.J., Ong, R.T., Suo, C. et al. (2011) Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. PLoS Genet., 7, e1002402.
-
(2011)
PLoS Genet.
, vol.7
-
-
Fan, Q.1
Zhou, X.2
Khor, C.C.3
Cheng, C.Y.4
Goh, L.K.5
Sim, X.6
Tay, W.T.7
Li, Y.J.8
Ong, R.T.9
Suo, C.10
-
8
-
-
77957557992
-
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
-
Hysi, P.G., Young, T.L., Mackey, D.A., Andrew, T., Fernandez-Medarde, A., Solouki, A.M., Hewitt, A.W., Macgregor, S., Vingerling, J.R., Li, Y.J. et al. (2010) A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nat. Genet., 42, 902-905.
-
(2010)
Nat. Genet.
, vol.42
, pp. 902-905
-
-
Hysi, P.G.1
Young, T.L.2
Mackey, D.A.3
Andrew, T.4
Fernandez-Medarde, A.5
Solouki, A.M.6
Hewitt, A.W.7
Macgregor, S.8
Vingerling, J.R.9
Li, Y.J.10
-
9
-
-
77957567357
-
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
-
Solouki, A.M., Verhoeven, V.J., van Duijn, C.M., Verkerk, A.J., Ikram, M.K., Hysi, P.G., Despriet, D.D., van Koolwijk, L.M., Ho, L., Ramdas,W.D. et al. (2010) A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Nat. Genet., 42, 897-901.
-
(2010)
Nat. Genet.
, vol.42
, pp. 897-901
-
-
Solouki, A.M.1
Verhoeven, V.J.2
Van Duijn, C.M.3
Verkerk, A.J.4
Ikram, M.K.5
Hysi, P.G.6
Despriet, D.D.7
Van Koolwijk, L.M.8
Ho, L.9
Ramdas, W.D.10
-
10
-
-
84874654256
-
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
-
Verhoeven, V.J., Hysi, P.G., Wojciechowski, R., Fan, Q., Guggenheim, J.A., Hohn, R., MacGregor, S., Hewitt, A.W., Nag, A., Cheng, C.Y. et al. (2013) Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet., 45, 314-318.
-
(2013)
Nat. Genet.
, vol.45
, pp. 314-318
-
-
Verhoeven, V.J.1
Hysi, P.G.2
Wojciechowski, R.3
Fan, Q.4
Guggenheim, J.A.5
Hohn, R.6
MacGregor, S.7
Hewitt, A.W.8
Nag, A.9
Cheng, C.Y.10
-
11
-
-
84878921285
-
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
-
Stambolian, D., Wojciechowski, R., Oexle, K., Pirastu, M., Li, X., Raffel, L.J., Cotch,M.F., Chew, E.Y., Klein, B., Klein, R. et al. (2013) Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum. Mol. Genet., 22, 2754-2764.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 2754-2764
-
-
Stambolian, D.1
Wojciechowski, R.2
Oexle, K.3
Pirastu, M.4
Li, X.5
Raffel, L.J.6
Cotch, M.F.7
Chew, E.Y.8
Klein, B.9
Klein, R.10
-
12
-
-
84868337361
-
Large-scale association analysis provides insights into the genetic architecture and patho physiology of type 2 diabetes
-
Morris, A.P., Voight, B.F., Teslovich, T.M., Ferreira, T., Segre, A.V., Steinthorsdottir, V., Strawbridge, R.J., Khan, H., Grallert, H.,Mahajan, A. et al. (2012) Large-scale association analysis provides insights into the genetic architecture and patho physiology of type 2 diabetes. Nat.Genet., 44, 981-990.
-
(2012)
Nat.Genet.
, vol.44
, pp. 981-990
-
-
Morris, A.P.1
Voight, B.F.2
Teslovich, T.M.3
Ferreira, T.4
Segre, A.V.5
Steinthorsdottir, V.6
Strawbridge, R.J.7
Khan, H.8
Grallert, H.9
Mahajan, A.10
-
13
-
-
79551516905
-
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese
-
Li, Y.J., Goh, L., Khor, C.C., Fan, Q., Yu, M., Han, S., Sim, X., Ong, R.T., Wong, T.Y., Vithana, E.N. et al. (2011) Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology, 118, 368-375.
-
(2011)
Ophthalmology
, vol.118
, pp. 368-375
-
-
Li, Y.J.1
Goh, L.2
Khor, C.C.3
Fan, Q.4
Yu, M.5
Han, S.6
Sim, X.7
Ong, R.T.8
Wong, T.Y.9
Vithana, E.N.10
-
14
-
-
70349667197
-
A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1
-
Nakanishi, H., Yamada, R., Gotoh, N., Hayashi, H., Yamashiro, K., Shimada, N., Ohno-Matsui, K., Mochizuki, M., Saito, M., Iida, T. et al. (2009) A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. PLoS Genet., 5, e1000660.
-
(2009)
PLoS Genet.
, vol.5
-
-
Nakanishi, H.1
Yamada, R.2
Gotoh, N.3
Hayashi, H.4
Yamashiro, K.5
Shimada, N.6
Ohno-Matsui, K.7
Mochizuki, M.8
Saito, M.9
Iida, T.10
-
15
-
-
84877928444
-
Agenome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
-
Shi, Y., Gong, B., Chen, L., Zuo, X., Liu, X., Tam, P.O., Zhou, X., Zhao, P., Lu, F., Qu, J. et al. (2013) Agenome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population. Hum. Mol. Genet., 22, 2325-2333.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 2325-2333
-
-
Shi, Y.1
Gong, B.2
Chen, L.3
Zuo, X.4
Liu, X.5
Tam, P.O.6
Zhou, X.7
Zhao, P.8
Lu, F.9
Qu, J.10
-
16
-
-
79958831466
-
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
-
Shi, Y., Qu, J., Zhang, D., Zhao, P., Zhang, Q., Tam, P.O., Sun, L., Zuo, X., Zhou, X., Xiao, X. et al. (2011) Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. Am. J. Hum. Genet., 88, 805-813.
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 805-813
-
-
Shi, Y.1
Qu, J.2
Zhang, D.3
Zhao, P.4
Zhang, Q.5
Tam, P.O.6
Sun, L.7
Zuo, X.8
Zhou, X.9
Xiao, X.10
-
17
-
-
84878569025
-
Genome-wideSNPandCNVanalysis identifiescommonand low-frequency variants associated with severe early-onset obesity
-
Wheeler, E., Huang, N., Bochukova, E.G., Keogh, J.M., Lindsay, S., Garg, S., Henning, E., Blackburn, H., Loos, R.J., Wareham, N.J. et al. (2013) Genome-wideSNPandCNVanalysis identifiescommonand low-frequency variants associated with severe early-onset obesity. Nat. Genet., 45, 513-517.
-
(2013)
Nat. Genet.
, vol.45
, pp. 513-517
-
-
Wheeler, E.1
Huang, N.2
Bochukova, E.G.3
Keogh, J.M.4
Lindsay, S.5
Garg, S.6
Henning, E.7
Blackburn, H.8
Loos, R.J.9
Wareham, N.J.10
-
18
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen, J.C., Kiss, R.S., Pertsemlidis, A., Marcel, Y.L., McPherson, R. and Hobbs, H.H. (2004) Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science, 305, 869-872.
-
(2004)
Science
, vol.305
, pp. 869-872
-
-
Cohen, J.C.1
Kiss, R.S.2
Pertsemlidis, A.3
Marcel, Y.L.4
McPherson, R.5
Hobbs, H.H.6
-
19
-
-
0037854588
-
The tree shrews:adjuncts and alternatives to primates as models for biomedical research
-
Cao, J., Yang, E.B., Su, J.J., Li, Y. and Chow, P. (2003) The tree shrews:adjuncts and alternatives to primates as models for biomedical research. J. Med. Primatol., 32, 123-130.
-
(2003)
J. Med. Primatol.
, vol.32
, pp. 123-130
-
-
Cao, J.1
Yang, E.B.2
Su, J.J.3
Li, Y.4
Chow, P.5
-
20
-
-
0033002171
-
Afocal magnification does not influence chick eye development
-
Curry, T.A., Sivak, J.G., Callender, M.G. and Irving, E.L. (1999) Afocal magnification does not influence chick eye development. Optom. Vis. Sci., 76, 316-319.
-
(1999)
Optom. Vis. Sci.
, vol.76
, pp. 316-319
-
-
Curry, T.A.1
Sivak, J.G.2
Callender, M.G.3
Irving, E.L.4
-
21
-
-
0036014915
-
Myopia and models and mechanisms of refractive error control
-
Lawrence, M.S. and Azar, D.T. (2002) Myopia and models and mechanisms of refractive error control. Ophthalmol. Clin. North. Am., 15, 127-133.
-
(2002)
Ophthalmol. Clin. North. Am.
, vol.15
, pp. 127-133
-
-
Lawrence, M.S.1
Azar, D.T.2
-
22
-
-
39949084856
-
Two models of experimental myopia in the mouse
-
Barathi, V.A., Boopathi, V.G., Yap, E.P. and Beuerman, R.W. (2008) Two models of experimental myopia in the mouse. Vis. Res., 48, 904-916.
-
(2008)
Vis. Res.
, vol.48
, pp. 904-916
-
-
Barathi, V.A.1
Boopathi, V.G.2
Yap, E.P.3
Beuerman, R.W.4
-
23
-
-
0037247617
-
Refractive changes induced by form deprivation in the mouse eye
-
Tejedor, J. and de la Villa, P. (2003) Refractive changes induced by form deprivation in the mouse eye. Invest. Ophthalmol. Vis. Sci., 44, 32-36.
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, pp. 32-36
-
-
Tejedor, J.1
De La Villa, P.2
-
24
-
-
1242341924
-
Measurement of refractive state and deprivation myopia in two strains of mice
-
Schaeffel, F., Burkhardt, E., Howland, H.C. and Williams, R.W. (2004) Measurement of refractive state and deprivation myopia in two strains of mice. Optom. Vis. Sci., 81, 99-110.
-
(2004)
Optom. Vis. Sci.
, vol.81
, pp. 99-110
-
-
Schaeffel, F.1
Burkhardt, E.2
Howland, H.C.3
Williams, R.W.4
-
25
-
-
34047235515
-
ZFHX1B mutations in patients with Mowat-Wilson syndrome
-
Dastot-Le Moal, F., Wilson, M., Mowat, D., Collot, N., Niel, F. and Goossens, M. (2007) ZFHX1B mutations in patients with Mowat-Wilson syndrome. Hum. Mutat., 28, 313-321.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 313-321
-
-
Dastot-Le Moal, F.1
Wilson, M.2
Mowat, D.3
Collot, N.4
Niel, F.5
Goossens, M.6
-
26
-
-
84878901270
-
ZEB2zinc-fingermissensemutations leadtohypomorphic alleles and a mild Mowat-Wilson syndrome
-
Ghoumid, J., Drevillon, L., Alavi-Naini, S.M., Bondurand, N., Rio, M., Briand-Suleau, A., Nasser, M., Goodwin, L., Raymond, P., Yanicostas, C. et al. (2013) ZEB2zinc-fingermissensemutations leadtohypomorphic alleles and a mild Mowat-Wilson syndrome. Hum. Mol. Genet., 22, 2652-2661.
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 2652-2661
-
-
Ghoumid, J.1
Drevillon, L.2
Alavi-Naini, S.M.3
Bondurand, N.4
Rio, M.5
Briand-Suleau, A.6
Nasser, M.7
Goodwin, L.8
Raymond, P.9
Yanicostas, C.10
-
27
-
-
84874654256
-
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
-
Verhoeven, V.J., Hysi, P.G., Wojciechowski, R., Fan, Q., Guggenheim, J.A., Hohn, R., MacGregor, S., Hewitt, A.W., Nag, A., Cheng, C.Y. et al. (2013) Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet., 45, 314-318.
-
(2013)
Nat. Genet.
, vol.45
, pp. 314-318
-
-
Verhoeven, V.J.1
Hysi, P.G.2
Wojciechowski, R.3
Fan, Q.4
Guggenheim, J.A.5
Hohn, R.6
MacGregor, S.7
Hewitt, A.W.8
Nag, A.9
Cheng, C.Y.10
-
28
-
-
84864051802
-
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia
-
Fan, Q., Barathi, V.A., Cheng, C.Y., Zhou, X., Meguro, A., Nakata, I., Khor, C.C., Goh, L.K., Li, Y.J., Lim, W. et al. (2012) Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. PLoS Genet., 8, e1002753.
-
(2012)
PLoS Genet.
, vol.8
-
-
Fan, Q.1
Barathi, V.A.2
Cheng, C.Y.3
Zhou, X.4
Meguro, A.5
Nakata, I.6
Khor, C.C.7
Goh, L.K.8
Li, Y.J.9
Lim, W.10
-
29
-
-
79959829340
-
Exome sequencing identifies ZNF644 mutations in high myopia
-
Shi, Y., Li, Y., Zhang, D., Zhang, H., Lu, F., Liu, X., He, F., Gong, B., Cai, L., Li, R. et al. (2011) Exome sequencing identifies ZNF644 mutations in high myopia. PLoS Genet., 7, e1002084.
-
(2011)
PLoS Genet.
, vol.7
-
-
Shi, Y.1
Li, Y.2
Zhang, D.3
Zhang, H.4
Lu, F.5
Liu, X.6
He, F.7
Gong, B.8
Cai, L.9
Li, R.10
-
30
-
-
7244255979
-
Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21
-
Gregory-Evans, C.Y., Vieira, H., Dalton, R., Adams, G.G., Salt, A. and Gregory-Evans, K. (2004) Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21. Am. J. Med. Genet. A, 131, 86-90.
-
(2004)
Am. J. Med. Genet. A
, vol.131
, pp. 86-90
-
-
Gregory-Evans, C.Y.1
Vieira, H.2
Dalton, R.3
Adams, G.G.4
Salt, A.5
Gregory-Evans, K.6
-
31
-
-
77958594059
-
beta2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granules
-
Schubert, S., Knoch, K.P., Ouwendijk, J.,Mohammed, S., Bodrov, Y., Jager, M., Altkruger, A., Wegbrod, C., Adams, M.E., Kim, Y. et al. (2010) beta2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granules. PLoS ONE, 5, e12929.
-
(2010)
PLoS ONE
, vol.5
-
-
Schubert, S.1
Knoch, K.P.2
Ouwendijk, J.3
Mohammed, S.4
Bodrov, Y.5
Jager, M.6
Altkruger, A.7
Wegbrod, C.8
Adams, M.E.9
Kim, Y.10
-
32
-
-
77955899173
-
The alpha-syntrophin PH and PDZ domains scaffold acetylcholine receptors, utrophin, and neuronal nitric oxide synthase at the neuromuscular junction
-
Adams, M.E., Anderson, K.N. and Froehner, S.C. (2010) The alpha-syntrophin PH and PDZ domains scaffold acetylcholine receptors, utrophin, and neuronal nitric oxide synthase at the neuromuscular junction. J. Neurosci., 30, 11004-11010.
-
(2010)
J. Neurosci.
, vol.30
, pp. 11004-11010
-
-
Adams, M.E.1
Anderson, K.N.2
Froehner, S.C.3
-
33
-
-
28244470066
-
Purification of ATP-binding cassette transporter A1 and associated binding proteins reveals the importance of beta1-syntrophin in cholesterol efflux
-
Okuhira, K., Fitzgerald,M.L., Sarracino,D.A.,Manning, J.J.,Bell, S.A., Goss, J.L. and Freeman, M.W. (2005) Purification of ATP-binding cassette transporter A1 and associated binding proteins reveals the importance of beta1-syntrophin in cholesterol efflux. J. Biol. Chem., 280, 39653-39664.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 39653-39664
-
-
Okuhira, K.1
Fitzgerald, M.L.2
Sarracino, D.A.3
Manning, J.J.4
Bell, S.A.5
Goss, J.L.6
Freeman, M.W.7
-
34
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M.A., Bender, D., Maller, J., Sklar, P., de Bakker, P.I., Daly, M.J. et al. (2007) PLINK:a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet., 81, 559-575.
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
-
35
-
-
59349110223
-
Effects of unilateral topical atropine on binocular pupil responses and eye growth in mice
-
Barathi, V.A., Beuerman, R.W. and Schaeffel, F. (2009) Effects of unilateral topical atropine on binocular pupil responses and eye growth in mice. Vision Res., 49, 383-387.
-
(2009)
Vision Res.
, vol.49
, pp. 383-387
-
-
Barathi, V.A.1
Beuerman, R.W.2
Schaeffel, F.3
|