Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia (Q57700508)

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Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia
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    Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia (English)
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    A. K. Erichsen
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    E. Inderhaug
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    K. Eiklid
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    C. M. E. Tallaksen
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    July 2007
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    14
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    7
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    809-814
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