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Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum

✍ Scribed by Alice Abdel Aleem; Nourhan Abu-Shahba; Dominika Swistun; Jennifer Silhavy; Stephanie L. Bielas; Shifteh Sattar; Joseph G. Gleeson; Maha S. Zaki

Book ID: 116433326
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 432 KB
Volume: 54
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2010.10.006

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