(Q46132585)
Statements
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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration (English)
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Hanna Orlén
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Atle Melberg
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Raili Raininko
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Eva Kumlien
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Miriam Entesarian
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Per Söderberg
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Magnus Påhlman
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Niklas Darin
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Mårten Kyllerman
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Eva Holmberg
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Henry Engler
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Urban Eriksson
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Niklas Dahl
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1 October 2009
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150B
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7
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984-992
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Identifiers
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