{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,3,28]],"date-time":"2024-03-28T18:33:52Z","timestamp":1711650832514},"reference-count":7,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurology"],"published-print":{"date-parts":[[1998,11]]},"DOI":"10.1212\/wnl.51.5.1509","type":"journal-article","created":{"date-parts":[[2012,5,13]],"date-time":"2012-05-13T13:36:49Z","timestamp":1336916209000},"page":"1509-1510","source":"Crossref","is-referenced-by-count":5,"title":["Analysis of microtubule-associated protein 1a gene in hereditary spastic paraplegia"],"prefix":"10.1212","volume":"51","author":[{"given":"S.","family":"Rainier","sequence":"first","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S. M.","family":"Jones","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Esposito","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Guice","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Otterud","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Leppert","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J. K.","family":"Fink","sequence":"additional","affiliation":[{"name":"From the Department of Neurology (Drs. Rainier and Fink, and S.M. Jones and E. Guice) and the DNA Sequencing Core Facility (C. Esposito), University of Michigan, Ann Arbor, MI; the Department of Human Genetics and the Eccles Institute of Human Genetics (Dr. Leppert and B. Otterud), University of Utah, Salt Lake City, UT; and the Geriatric Research, Education, and Care Center (Dr. Fink), Ann Arbor Veteran's Affairs Medical Center, MI."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"e_1_3_1_2_2","first-page":"2","volume":"11","year":"1988","unstructured":"Matus A. Microtubule-associated proteins: their potential role in determining neuronal morphology. Ann Rev Neurosci 1988;11:29-44.","journal-title":"Ann Rev Neurosci"},{"key":"e_1_3_1_3_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.46.1.1"},{"key":"e_1_3_1_4_2","first-page":"2","volume":"22","year":"1994","unstructured":"Lien LL, Feener CA, Fischbach N, Kunkel LM. Cloning of human microtubule-associated protein 1B and the identification of a related gene on chromosome 15. Genomics 1994;22:273-280.","journal-title":"Genomics"},{"key":"e_1_3_1_5_2","first-page":"3","volume":"45","year":"1995","unstructured":"Fink JK, Sharp G, Lange B, et al. Autosomal dominant hereditary spastic paraparesis, type I: clinical and genetic analysis of a large North American family. Neurology 1995;45:325-331.","journal-title":"Neurology"},{"key":"e_1_3_1_6_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320560102"},{"key":"e_1_3_1_7_2","first-page":"5","volume":"35","year":"1996","unstructured":"Fink JK, Jones SM, Esposito C, Wilkowski J. Human microtubule associated protein 1a (MAP1a): genomic organization, cDNA sequence, tissue specific expression. Genomics 1996;35:577-585.","journal-title":"Genomics"},{"key":"e_1_3_1_8_2","first-page":"6","volume":"48","year":"1991","unstructured":"Feener CA, Boyce FM, Kunkel LM. Rapid detection of CA polymorphisms in cloned DNA: application to the 5\u2032 region of the dystrophin gene. Am J Hum Genet 1991;48:621-627.","journal-title":"Am J Hum Genet"}],"container-title":["Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.neurology.org\/doi\/pdfdirect\/10.1212\/WNL.51.5.1509","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,3,27]],"date-time":"2024-03-27T16:05:42Z","timestamp":1711555542000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.neurology.org\/doi\/10.1212\/WNL.51.5.1509"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1998,11]]},"references-count":7,"journal-issue":{"issue":"5","published-print":{"date-parts":[[1998,11]]}},"alternative-id":["10.1212\/WNL.51.5.1509"],"URL":"https:\/\/doi.org\/10.1212\/wnl.51.5.1509","relation":{},"ISSN":["0028-3878","1526-632X"],"issn-type":[{"value":"0028-3878","type":"print"},{"value":"1526-632X","type":"electronic"}],"subject":[],"published":{"date-parts":[[1998,11]]}}}