{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T23:28:39Z","timestamp":1791156519514,"version":"4.1.0"},"publisher-location":"New York, NY","reference-count":28,"publisher":"Springer New York","isbn-type":[{"value":"9781441913982","type":"print"},{"value":"9781441913999","type":"electronic"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010]]},"DOI":"10.1007\/978-1-4419-1399-9_63","type":"book-chapter","created":{"date-parts":[[2010,2,8]],"date-time":"2010-02-08T18:14:47Z","timestamp":1265652887000},"page":"549-558","source":"Crossref","is-referenced-by-count":25,"title":["Congenital Stationary Night Blindness in Mice \u2013 A Tale of Two Cacna1f Mutants"],"prefix":"10.1007","author":[{"given":"N.","family":"Lodha","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Bonfield","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N.C.","family":"Orton","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C.J.","family":"Doering","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J.E.","family":"McRory","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.C.","family":"Mema","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R.","family":"Rehak","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y.","family":"Sauv\u00e9","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R.","family":"Tobias","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"W.K.","family":"Stell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N.T.","family":"Bech-Hansen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2009,12,28]]},"reference":[{"key":"63_CR1","doi-asserted-by":"crossref","first-page":"439","DOI":"10.1007\/978-1-4615-0121-3_26","volume":"514","author":"SL Ball","year":"2002","unstructured":"Ball SL, Gregg RG (2002) Using mutant mice to study the role of voltage-gated calcium channels in the retina. Adv Exp Med Biol 514:439\u2013450","journal-title":"Adv Exp Med Biol"},{"issue":"2","key":"63_CR2","doi-asserted-by":"publisher","first-page":"708","DOI":"10.1167\/iovs.03-0937","volume":"45","author":"L Baumann","year":"2004","unstructured":"Baumann L, Gerstner A et al (2004) Functional characterization of the L-type Ca2+ channel Cav1.4alpha1 from mouse retina. Invest Ophthalmol Vis Sci 45(2):708\u2013713","journal-title":"Invest Ophthalmol Vis Sci"},{"issue":"2","key":"63_CR3","doi-asserted-by":"publisher","first-page":"286","DOI":"10.1002\/cne.21188","volume":"500","author":"PR Bayley","year":"2007","unstructured":"Bayley PR, Morgans CW (2007) Rod bipolar cells and horizontal cells form displaced synaptic contacts with rods in the outer nuclear layer of the nob2 retina. J Comp Neurol 500(2):286\u2013298","journal-title":"J Comp Neurol"},{"issue":"3","key":"63_CR4","doi-asserted-by":"publisher","first-page":"264","DOI":"10.1038\/947","volume":"19","author":"NT Bech-Hansen","year":"1998","unstructured":"Bech-Hansen NT, Naylor MJ et al (1998) Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Nat Genet 19(3):264\u2013267","journal-title":"Nat Genet"},{"key":"63_CR5","unstructured":"5. Bonfield S, Tejedor J et al (2007) Spatiotemporal contrast sensitivity characteristics of optokinetic responses in chicks and in normal and Cacna1f-mutant mice, Invest Ophthalmol Vis Sci: (ARVO Abstracts), Program #2988"},{"key":"63_CR6","unstructured":"Bonfield S, Tejedor J et al (2009) Spatiotemporal contrast sensitivity characteristics of optokinetic responses in chicks and in normal and Cacna1f-mutant mice in neuroscience. University of Calgary."},{"issue":"4","key":"63_CR7","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1016\/S0008-4182(00)80031-9","volume":"35","author":"KM Boycott","year":"2000","unstructured":"Boycott KM, Pearce WG et al (2000) Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in Cacna1f. Can J Ophthalmol 35(4):204\u2013213","journal-title":"Can J Ophthalmol"},{"issue":"5","key":"63_CR8","doi-asserted-by":"publisher","first-page":"587","DOI":"10.1017\/S0952523805225075","volume":"22","author":"B Chang","year":"2005","unstructured":"Chang B, Hawes NL et al (2005) Mouse models of ocular diseases. Vis Neurosci 22(5):587\u2013593","journal-title":"Vis Neurosci"},{"issue":"1","key":"63_CR9","doi-asserted-by":"publisher","first-page":"11","DOI":"10.1017\/S095252380623102X","volume":"23","author":"B Chang","year":"2006","unstructured":"Chang B, Heckenlively JR et al (2006) The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Vis Neurosci 23(1):11\u201324","journal-title":"Vis Neurosci"},{"issue":"5","key":"63_CR10","doi-asserted-by":"publisher","first-page":"775","DOI":"10.1016\/S0896-6273(03)00086-2","volume":"37","author":"O Dick","year":"2003","unstructured":"Dick O, tom Dieck C et al (2003) The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina. Neuron 37(5):775\u2013786","journal-title":"Neuron"},{"issue":"7","key":"63_CR11","doi-asserted-by":"publisher","first-page":"e2538","DOI":"10.1371\/journal.pone.0002538","volume":"3","author":"CJ Doering","year":"2008","unstructured":"Doering CJ, Rehak R et al (2008) Modified Ca(v)1.4 expression in the Cacna1f(nob2) mouse due to alternative splicing of an ETn inserted in exon 2. PLoS ONE 3(7):e2538","journal-title":"PLoS ONE"},{"issue":"10","key":"63_CR12","doi-asserted-by":"publisher","first-page":"1079","DOI":"10.1038\/nn1320","volume":"7","author":"F Haeseleer","year":"2004","unstructured":"Haeseleer F, Imanishi Y et al (2004) Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function. Nat Neurosci 7(10):1079\u20131087","journal-title":"Nat Neurosci"},{"issue":"1","key":"63_CR13","doi-asserted-by":"publisher","first-page":"85","DOI":"10.1016\/S0896-6273(00)00011-8","volume":"27","author":"S Haverkamp","year":"2000","unstructured":"Haverkamp S, Gr\u00fcnert U et al (2000) The cone pedicle, a complex synapse in the retina. Neuron 27(1):85\u201395","journal-title":"Neuron"},{"issue":"1","key":"63_CR14","doi-asserted-by":"publisher","first-page":"252","DOI":"10.1523\/JNEUROSCI.3054-04.2005","volume":"25","author":"JC Hoda","year":"2005","unstructured":"Hoda JC, Zaghetto F et al (2005) Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels. J Neurosci 25(1):252\u2013259","journal-title":"J Neurosci"},{"key":"63_CR15","unstructured":"Lodha N et al (2009) Phenotypic variability in genetically defined X-linked congenital stationary night blindness. Investigative Ophthalmology and Vis Sci Invest Ophthalmol, p. (ARVO Abstracts), Program # 3721"},{"issue":"20","key":"63_CR16","doi-asserted-by":"publisher","first-page":"3035","DOI":"10.1093\/hmg\/ddi336","volume":"14","author":"F Mansergh","year":"2005","unstructured":"Mansergh F, Orton NC et al (2005) Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina. Hum Mol Genet 14(20):3035\u20133046","journal-title":"Hum Mol Genet"},{"issue":"7","key":"63_CR17","doi-asserted-by":"publisher","first-page":"1707","DOI":"10.1523\/JNEUROSCI.4846-03.2004","volume":"24","author":"JE McRory","year":"2004","unstructured":"McRory JE, Hamid J et al (2004) The Cacna1f gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution. J Neurosci 24(7):1707\u20131718","journal-title":"J Neurosci"},{"issue":"12","key":"63_CR18","first-page":"737","volume":"106","author":"Y Miyake","year":"2002","unstructured":"Miyake Y (2002) Establishment of the concept of new clinical entities-complete and incomplete form of congenital stationary night blindness. Nippon Ganka Gakkai Zasshi 106(12):737\u2013755; discussion 756","journal-title":"Nippon Ganka Gakkai Zasshi"},{"issue":"7","key":"63_CR19","doi-asserted-by":"crossref","first-page":"1013","DOI":"10.1001\/archopht.1986.01050190071042","volume":"104","author":"Y Miyake","year":"1986","unstructured":"Miyake Y, Yagasaki K et al (1986) Congenital stationary night blindness with negative electroretinogram. A new classification. Arch Ophthalmol 104(7):1013\u20131020","journal-title":"Arch Ophthalmol"},{"issue":"5","key":"63_CR20","doi-asserted-by":"publisher","first-page":"561","DOI":"10.1017\/S0952523805225038","volume":"22","author":"CW Morgans","year":"2005","unstructured":"Morgans CW, Bayley PR et al (2005) Photoreceptor calcium channels: insight from night blindness. Vis Neurosci 22(5):561\u2013568","journal-title":"Vis Neurosci"},{"key":"63_CR21","volume-title":"The Cacna1f-Mutant Retina Shows Evidence of Failed Synaptogenesis, Abnormal Synaptic Ribbon Structure and Increased Photoreceptor Cell Death","author":"NC Orton","year":"2007","unstructured":"Orton NC, Stell WK, Bech-Hansen NT (2007) The Cacna1f-Mutant Retina Shows Evidence of Failed Synaptogenesis, Abnormal Synaptic Ribbon Structure and Increased Photoreceptor Cell Death. Investigative Ophthalmology and Visual Science Invest Ophthalmol, p. (ARVO Abstract), Program # 4466"},{"issue":"2","key":"63_CR22","doi-asserted-by":"publisher","first-page":"335","DOI":"10.1016\/j.neuroscience.2007.09.021","volume":"150","author":"JB Peloquin","year":"2007","unstructured":"Peloquin JB, Rehak R et al (2007) Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W. Neuroscience 150(2): 335\u2013345","journal-title":"Neuroscience"},{"issue":"28","key":"63_CR23","doi-asserted-by":"publisher","first-page":"3411","DOI":"10.1016\/j.visres.2004.09.001","volume":"44","author":"GT Prusky","year":"2004","unstructured":"Prusky GT, Douglas RM (2004) Characterization of mouse cortical spatial vision. Vis Res 44(28):3411\u20133418","journal-title":"Vis Res"},{"issue":"5","key":"63_CR24","doi-asserted-by":"publisher","first-page":"745","DOI":"10.1002\/cne.21526","volume":"506","author":"ME Raven","year":"2008","unstructured":"Raven ME, Orton NC et al (2008) Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology. J Comp Neurol 506(5):745\u2013758","journal-title":"J Comp Neurol"},{"issue":"3","key":"63_CR25","doi-asserted-by":"publisher","first-page":"260","DOI":"10.1038\/940","volume":"19","author":"TM Strom","year":"1998","unstructured":"Strom TM, Nyakatura G et al (1998) An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet 19(3):260\u2013263","journal-title":"Nat Genet"},{"issue":"16","key":"63_CR26","doi-asserted-by":"publisher","first-page":"2383","DOI":"10.1016\/0042-6989(95)00006-L","volume":"35","author":"F Tremblay","year":"1995","unstructured":"Tremblay F, Laroche RG et al (1995) The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness. Vis Res 35(16):2383\u20132393","journal-title":"Vis Res"},{"issue":"1","key":"63_CR27","doi-asserted-by":"publisher","first-page":"189","DOI":"10.1523\/JNEUROSCI.3551-07.2008","volume":"28","author":"Y Umino","year":"2008","unstructured":"Umino Y, Solessio E et al (2008) Speed, spatial, and temporal tuning of rod and cone vision in mouse. J Neurosci 28(1):189\u2013198","journal-title":"J Neurosci"},{"issue":"1","key":"63_CR28","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1097\/MOH.0b013e3282f13cd2","volume":"15","author":"J Xia","year":"2008","unstructured":"Xia J, Link DC (2008) Severe congenital neutropenia and the unfolded protein response. Curr Opin Hematol 15(1):1\u20137","journal-title":"Curr Opin Hematol"}],"container-title":["Advances in Experimental Medicine and Biology","Retinal Degenerative Diseases"],"original-title":[],"link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/978-1-4419-1399-9_63.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,11,18]],"date-time":"2020-11-18T05:10:29Z","timestamp":1605676229000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/978-1-4419-1399-9_63"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,12,28]]},"ISBN":["9781441913982","9781441913999"],"references-count":28,"URL":"https:\/\/doi.org\/10.1007\/978-1-4419-1399-9_63","relation":{},"ISSN":["0065-2598"],"issn-type":[{"value":"0065-2598","type":"print"}],"subject":[],"published":{"date-parts":[[2009,12,28]]}}}