(Q47751582)
Statements
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Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype (English)
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B N Smith
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S Bevan
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C Vance
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P Renwick
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P Wilkinson
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C Proukakis
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F Squitieri
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A Berardelli
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T T Warner
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E Reid
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C E Shaw
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1 May 2009
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75
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5
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485-489
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