Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum
| Autor: | Aleem, Alice Abdel, Abu-Shahba, Nourhan, Swistun, Dominika, Silhavy, Jennifer, Bielas, Stephanie L., Sattar, Shifteh, Gleeson, Joseph G., Zaki, Maha S. |
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| Zdroj: | In European Journal of Medical Genetics 2011 54(1):82-85 |
| Databáze: | ScienceDirect |
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