Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. (Q48081283)

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scientific article published on 18 February 2007
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Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
scientific article published on 18 February 2007

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    Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. (English)
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