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A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2

✍ Scribed by Noetzli, Leila; Sanz, Pablo G.; Brodsky, Gary L.; Hinckley, Jesse D.; Giugni, Juan C.; Giannaula, Rolando J.; Gonzalez-Alegre, Pedro; Di Paola, Jorge

Book ID: 121959346
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 701 KB
Volume: 533
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.09.076

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