{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,25]],"date-time":"2023-09-25T14:26:29Z","timestamp":1695651989173},"reference-count":45,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1992,1,1]],"date-time":"1992-01-01T00:00:00Z","timestamp":694224000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Mammalian Genome"],"published-print":{"date-parts":[[1992]]},"DOI":"10.1007\/bf00352459","type":"journal-article","created":{"date-parts":[[2004,10,31]],"date-time":"2004-10-31T03:37:59Z","timestamp":1099193879000},"page":"151-155","source":"Crossref","is-referenced-by-count":10,"title":["The ?-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse Chromosome 11"],"prefix":"10.1007","volume":"3","author":[{"given":"Christine","family":"Ambrose","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shirley","family":"Cheng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bertrand","family":"Fontaine","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joseph H.","family":"Nadeau","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marcy","family":"MacDonald","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James F.","family":"Gusella","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1146\/annurev.ne.11.030188.002323","volume":"11","author":"R.L. Barchi","year":"1988","unstructured":"Barchi, R.L.: Probing the molecular structure of the voltage-dependent sodium channel. Annu Rev Neurosci 11: 455?495, 1988.","journal-title":"Annu Rev Neurosci"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"S158","DOI":"10.1007\/BF00656492","volume":"1","author":"A.M. Buchberg","year":"1991","unstructured":"Buchberg, A.M., Moskow, J.J., Buckwalter, M.S., and Camper, S.A.: Mouse Chromosome 11. Mammalian Genome 1 (Suppl): S158-S191, 1991.","journal-title":"Mammalian Genome"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"619","DOI":"10.1016\/0896-6273(91)90064-7","volume":"6","author":"S.C. Cannon","year":"1991","unstructured":"Cannon, S.C., Brown, R.H. Jr., and Corey, D.P.: A sodium channel defect in hyperkalemic paralysis. Neuron 6: 619?626, 1991.","journal-title":"Neuron"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1126\/science.2459775","volume":"242","author":"W.A. Catterall","year":"1988","unstructured":"Catterall, W.A.: Structure and function of voltage-sensitive ion channels. Science 242: 50?61, 1988.","journal-title":"Science"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"401","DOI":"10.1089\/dna.1987.6.401","volume":"6","author":"S.V. Cheng","year":"1987","unstructured":"Cheng, S.V., Lugo, T.G., Tanzi, R.E., Whitney III, J.B., Fournier, R.E.K., and Gusella, J.F.: Chromosomal localization of the mouse homologue of the Huntington's disease-linked G8 (D4S10) marker. DNA 6: 401?407, 1987.","journal-title":"DNA"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1007\/BF02982178","volume":"38","author":"F.A.E. Crew","year":"1939","unstructured":"Crew, F.A.E. and Auerbach, C.: A dominant autosomal monogenic coat texture character in the mouse. J Genet 38: 341?344, 1939.","journal-title":"J Genet"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"591","DOI":"10.1016\/0888-7543(90)90051-U","volume":"8","author":"R.W. Elliott","year":"1990","unstructured":"Elliott, R.W., Lee, B.K., and Eicher, E.M.: Localization of the growth hormone gene to the distal half of mouse chromosome 11. Genomics 8: 591?594, 1990.","journal-title":"Genomics"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"192","DOI":"10.1007\/BF02996215","volume":"50","author":"D.S. Falconer","year":"1951","unstructured":"Falconer, D.S.: Two new mutants, trembler and reeler, with neurological actions in the house mouse (Mus musculus L.) J Genet 50: 192?201, 1951.","journal-title":"J Genet"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1016\/0003-2697(83)90418-9","volume":"132","author":"A.P. Feinberg","year":"1983","unstructured":"Feinberg, A.P. and Vogelstein, B.: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Ann Biochem 132: 6?13, 1983.","journal-title":"Ann Biochem"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"1000","DOI":"10.1126\/science.2173143","volume":"250","author":"B. Fontaine","year":"1990","unstructured":"Fontaine, B., Khurana, T.S., Hoffman, E.P., Bruns, G.A.P., Haines, J.L., Trofatter, J.A., Hanson, M.P., Rich, J., McFarlane, H., McKenna Yasek, D., Romano, D., Gusella, J.F., and Brown, R.H. Jr.: Hyperkalemic periodic paralysis and the adult muscle sodium channel ?-subunit gene. Science 250: 1000?1002, 1990.","journal-title":"Science"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1016\/0888-7543(91)90425-E","volume":"9","author":"A.L. George","year":"1991","unstructured":"George, A.L., Ledbetter, D.H., Kallen, R.G., and Barchi, R.L.: Assignment of a human skeletal muscle sodium channel ?-subunit gene (SCN4A) to 17q23.1?q25.3. Genomics 9: 555?556, 1991.","journal-title":"Genomics"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1093\/oxfordjournals.jhered.a107548","volume":"58","author":"E.L. Green","year":"1967","unstructured":"Green, E.L.: Shambling, a neurological mutant of the mouse. J Hered 58: 65?68, 1967.","journal-title":"J Hered"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1093\/oxfordjournals.jhered.a107077","volume":"52","author":"E.L. Green","year":"1968","unstructured":"Green, E.L.: Linkage of shambling with rex in linkage group VII of the mouse. J Hered 52: 223?227, 1968.","journal-title":"J Hered"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1016\/0027-5107(71)90016-9","volume":"12","author":"E.L. Green","year":"1971","unstructured":"Green, E.L.: Fitness of heterozygotes of deleterious recessive mutations in the mouse. Mutat Res 12: 281?289, 1971.","journal-title":"Mutat Res"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/0888-7543(90)90218-J","volume":"8","author":"J.L. Haines","year":"1990","unstructured":"Haines, J.L., Ozelius, L.J., McFarlane, H., Menon, A., Tzall, S., Martiniuk, F., Hirschhorn, R., and Gusella, J.F.: A genetic linkage map of chromosome 17. Genomics 8: 1?6, 1990.","journal-title":"Genomics"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1073\/pnas.88.2.335","volume":"88","author":"J. Han","year":"1991","unstructured":"Han, J., Lu, C.M., Brown, G.B., and Rado, T.A.: Direct amplification of a single dissected chromosomal segment by polymerase chain reaction: a human brain sodium channel gene is on chromosome 2q22?q23. Proc Natl Acad Sci USA 88: 335?339, 1991.","journal-title":"Proc Natl Acad Sci USA"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"827","DOI":"10.1016\/0888-7543(91)90469-U","volume":"10","author":"J. Hozier","year":"1991","unstructured":"Hozier, J., Scalzi, J., Sawyer, J., Carley, N., Applegate, M., Clive, D., and Moore, M.M.: Localization of the mouse thymidine kinase gene to the distal portion of chromosome 11. Genomics 10: 827?830, 1991.","journal-title":"Genomics"},{"key":"CR18","doi-asserted-by":"crossref","first-page":"2462","DOI":"10.1210\/endo-122-6-2462","volume":"122","author":"L.L. Jackson-Grusby","year":"1988","unstructured":"Jackson-Grusby, L.L., Pravtcheva, D., Ruddle, F.H., and Linzer, D.I.H.: Chromosomal mapping of the prolactin\/growth hormone gene family in the mouse. Endocrinology 122: 2462?2466, 1988.","journal-title":"Endocrinology"},{"key":"CR19","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1016\/0896-6273(90)90098-Z","volume":"4","author":"R.G. Kallen","year":"1990","unstructured":"Kallen, R.G., Sheng, Z.H., Yang, J., Chen, L.Q., Rogart, B., and Barchi, R.L.: Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle. Neuron 4: 233?242, 1990.","journal-title":"Neuron"},{"key":"CR20","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1016\/0014-5793(88)80614-8","volume":"228","author":"T. Kayano","year":"1988","unstructured":"Kayano, T., Noda, M., Flockerzi, V., Takahashi, H., and Numa, S.: Primary structure of rat brain sodium channel III deduced from the cDNA sequence. FEBS Lett 228: 187?194, 1988.","journal-title":"FEBS Lett"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"583","DOI":"10.1136\/jmg.28.9.583","volume":"28","author":"M.C. Koch","year":"1991","unstructured":"Koch, M.C., Ricker, K., Otto, M., Grimm, T., Hoffman, E.P., Rudel, R., Bender, K., Zoll, B., Harper, P.S., and Lehmann-Horn, F.: Confirmation of linkage of hyperkalemic periodic paralysis to chromosome 17. J Med Genet 28: 583?586, 1991a.","journal-title":"J Med Genet"},{"key":"CR22","doi-asserted-by":"crossref","first-page":"71","DOI":"10.1007\/BF00204932","volume":"88","author":"M.C. Koch","year":"1991","unstructured":"Koch, M.C., Ricker, K., Otto, M., Grimm, T., Bender, K., Zoll, B., Harper, P.S., Lehmann-Horn, F., Rudel, R., and Hoffman, E.P.: Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Hum Genet 88: 71?74, 1991b.","journal-title":"Hum Genet"},{"key":"CR23","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1007\/BF01551809","volume":"3","author":"C. Kozak","year":"1977","unstructured":"Kozak, C. and Ruddle, F.: Assignment of the genes for thymidine kinase and galactokinase to Mus musculus chromosome 11 and the preferential segregation of this chromosome in Chinese hamster\/mouse somatic cell hybrids. Somatic Cell Genet 3: 121?131, 1977.","journal-title":"Somatic Cell Genet"},{"key":"CR24","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1002\/mus.880100414","volume":"10","author":"F. Lehmann-Horn","year":"1987","unstructured":"Lehmann-Horn, F., Kuther, G., Ricker, K., Grafe, P., Ballanyi, K., and Rudel, R.: Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH. Muscle Nerve 10: 363?374, 1987a.","journal-title":"Muscle Nerve"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"633","DOI":"10.1002\/mus.880100709","volume":"10","author":"F. Lehman-Horn","year":"1987","unstructured":"Lehman-Horn, F., Rudel, R., and Ricker, K.: Membrane defects in paramyotonia congenita (Eulenburg). Muscle Nerve 10: 633?641, 1987b.","journal-title":"Muscle Nerve"},{"key":"CR26","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1007\/BF00370530","volume":"418","author":"F. Lehmann-Horn","year":"1991","unstructured":"Lehmann-Horn, F., Iaizzo, P.A., Hatt, H., and Franke, C.: Altered single Na+ channel conductance and gating in hyperkalemic periodic paralysis. Pflugers Arch 418: 297?299, 1991.","journal-title":"Pflugers Arch"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"3149","DOI":"10.1128\/MCB.5.11.3149","volume":"5","author":"P.F. Lin","year":"1985","unstructured":"Lin, P.F., Lieberman, H.B., Yeh, D.B., Xu, T., Zhao, T.Y., and Ruddle, F.H.: Molecular cloning and structural analysis of murine thymidine kinase genomic and cDNA sequences. Mol Cell Biol 5: 3149?3156, 1985.","journal-title":"Mol Cell Biol"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1016\/0888-7543(89)90047-5","volume":"5","author":"M. Litt","year":"1989","unstructured":"Litt, M., Luty, J., Kwak, M., Allen, L., Magenis, R.E., and Mandel G.: Localization of a human brain sodium channel gene (SCN2A) to chromosome 2. Genomics 5: 204?208, 1989.","journal-title":"Genomics"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"666","DOI":"10.1016\/0888-7543(91)90450-S","volume":"10","author":"D. Malo","year":"1991","unstructured":"Malo, D., Schurr, E., Dorfman, J., Canfield, V., Levenson, R., and Gros, P.: Three brain sodium channel ?-subunit genes are clustered on the proximal segment of mouse chromosome 2. Genomics 10: 666?672, 1991.","journal-title":"Genomics"},{"key":"CR30","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1007\/BF00352337","volume":"1","author":"F. Martiniuk","year":"1991","unstructured":"Martiniuk, F., Hirschhorn R., and D'Eustachio, P.: Linkage of acid ?-glucosidase (Gaa) and thymidine kinase (Tk-1) to esterase-3 (Es-3) on mouse Chromosome 11. Mammalian Genome 1: 267?269, 1991.","journal-title":"Mammalian Genome"},{"key":"CR31","unstructured":"McClatchey, A.I., Trofatter, J., McKenna-Yasek, D., Raskind, W., Bird, T., Pericak-Vance, M., Gilchrist, J., Arahata, K., Radosavljevic D., Van den Bergh, P., Haines, J.L., Gusella, J.F., and Brown, R.H. Jr.: Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita. Am J Hum Genet, in press, 1992."},{"key":"CR32","doi-asserted-by":"crossref","first-page":"620","DOI":"10.1097\/00005072-196710000-00008","volume":"26","author":"H. Meier","year":"1967","unstructured":"Meier, H.: Pathological findings in shambling, a hereditary neuropathy of mice. J Neuropathol Exp Neurol 26: 620?627, 1967.","journal-title":"J Neuropathol Exp Neurol"},{"key":"CR33","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1017\/S0016672300022242","volume":"45","author":"J.H. Nadeau","year":"1985","unstructured":"Nadeau, J.H., Philips, S.J., and Egorov, I.K.: Recombination between the t 6 complex and linked loci in the house mouse. Gene Res 45: 251?264, 1985.","journal-title":"Gene Res"},{"key":"CR34","doi-asserted-by":"crossref","first-page":"454","DOI":"10.1016\/0888-7543(89)90009-8","volume":"5","author":"J.H. Nadeau","year":"1989","unstructured":"Nadeau, J.H., Berger, F.G., Cox, D.R., Crosby, J.L., Davisson, M.T., Ferrara, D., Fuchs, E., Hart, C., Hunihan, L., Lalley, P.A., Langley, S.H., Martin, G.R., Nichols, L., Phillips, S.J., Roderick, T.H., Roop, D.R., Ruddle, F.H., Skow, L.C., and Compton, J.G.: A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the Rex locus on mouse chromosome 11. Genomics 5: 454?462, 1989.","journal-title":"Genomics"},{"key":"CR35","doi-asserted-by":"crossref","first-page":"469","DOI":"10.1016\/0888-7543(90)90033-Q","volume":"8","author":"J.H. Nadeau","year":"1990","unstructured":"Nadeau, J.H., Birkenmeir, C.S., Chowdhury, K., Crosby, J.L., and Lalley, P.A.: Zine finger protein gene complexes on mouse Chromosomes 8 and 11. Genomics 8: 469?476, 1990.","journal-title":"Genomics"},{"key":"CR36","doi-asserted-by":"crossref","first-page":"826","DOI":"10.1038\/322826a0","volume":"322","author":"M. Noda","year":"1986","unstructured":"Noda, M., Ikeda, T., Suzuki, H., Takeshima, H., Takahashi, T., Kuno, M., and Numa, S.: Expression of functional sodium channels from cloned cDNA. Nature 322: 826?828, 1986a.","journal-title":"Nature"},{"key":"CR37","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1038\/320188a0","volume":"320","author":"M. Noda","year":"1986","unstructured":"Noda, M., Ikeda, T., Kayano, T., Suzuki, H., Takeshima, H., Kurasaki, M., Takahashi, H., and Numa, S.: Existence of distinct sodium channel messenger RNAs in rat brain. Nature 320: 188?192, 1986b.","journal-title":"Nature"},{"key":"CR38","first-page":"378","volume":"49","author":"L.J. Ptacek","year":"1991","unstructured":"Ptacek, L.J., Tyler, F., Trimmer, J.S., and Leppert, M.: Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus. Am J Hum Genet 49: 378?382, 1991a.","journal-title":"Am J Hum Genet"},{"key":"CR39","first-page":"851","volume":"49","author":"L.J. Ptacek","year":"1991","unstructured":"Ptacek, L.J., Trimmer, J.S., Agnew, W.S., Roberts, J.W., Petajan, J.H., and Leppert, M.: Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium channel gene locus. Am J Hum Genet 49: 851?854, 1991b.","journal-title":"Am J Hum Genet"},{"key":"CR40","doi-asserted-by":"crossref","first-page":"1021","DOI":"10.1016\/0092-8674(91)90374-8","volume":"67","author":"L.J. Ptacek","year":"1991","unstructured":"Ptacek, L.J., George, A.L. Jr., Griggs, R.C., Tawil, R., Kallen, R.G., Barchi, R.L., Robertson, M., and Leppert, M.: Identification of a mutation in the gene causing hyperkalemic periodic paralysis. Cell 67: 1021?1027, 1991c.","journal-title":"Cell"},{"key":"CR41","doi-asserted-by":"crossref","first-page":"8170","DOI":"10.1073\/pnas.86.20.8170","volume":"86","author":"R.B. Rogart","year":"1989","unstructured":"Rogart, R.B., Cribbs, L.L., Muglia, L.K., Kephart, D., and Kaiser, M.W.: Molecular cloning of a putative terodotixin-resistant rat heart Na+ channel isoform. Proc Natl Acad Sci USA 86: 8170?8174, 1989.","journal-title":"Proc Natl Acad Sci USA"},{"key":"CR42","doi-asserted-by":"crossref","first-page":"387","DOI":"10.1038\/354387a0","volume":"354","author":"C.V. Rojas","year":"1991","unstructured":"Rojas, C.V., Wang, J., Hoffman, E.P., Powell, B.R., and Brown, R.H.: A methionine to valine mutation in the skeletal muscle sodium channel ?-subunit in human hyperkalemic periodic paralysis. Nature 354: 387?389, 1991.","journal-title":"Nature"},{"key":"CR43","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1093\/nar\/17.1.185","volume":"17","author":"C. Seiser","year":"1989","unstructured":"Seiser, C., Knofler, M., Rudelstorfer, I., Haas, R., and Wintersberger, E.: Mouse thymidine kinase: the promoter sequence and the gene and pseudogene structures in normal cells and in thymidine kinase deficient mutants. Nucleic Acids Res 17: 185?195, 1989.","journal-title":"Nucleic Acids Res"},{"key":"CR44","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1159\/000132797","volume":"51","author":"E. Solomon","year":"1989","unstructured":"Solomon, E. and Barker, D.F.: Report of the committee on the genetic constitution of chromosome 17. Cytogenet Cell Genet 51: 319?337, 1989.","journal-title":"Cytogenet Cell Genet"},{"key":"CR45","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1016\/0896-6273(89)90113-X","volume":"3","author":"J.S. Trimmer","year":"1989","unstructured":"Trimmer, J.S., Cooperman, S.S., Tomiko, S.A., Zhou, J., Crean, S.M., Boyle, M.B., Kallen, R.G., Sheng, Z., Barchi, R.L., Sigworth, F.J., Goodman, R.H., Agnew, W.S., and Mandel, G.: Primary structure and expression of a mammalian skeletal muscle sodium channel. Neuron 3: 33?49, 1989.","journal-title":"Neuron"}],"container-title":["Mammalian Genome"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00352459.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00352459\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00352459","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,8]],"date-time":"2019-04-08T23:47:12Z","timestamp":1554767232000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00352459"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1992]]},"references-count":45,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1992]]}},"alternative-id":["BF00352459"],"URL":"https:\/\/doi.org\/10.1007\/bf00352459","relation":{},"ISSN":["0938-8990","1432-1777"],"issn-type":[{"value":"0938-8990","type":"print"},{"value":"1432-1777","type":"electronic"}],"subject":[],"published":{"date-parts":[[1992]]}}}