KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations (Q35969072)

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KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations
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    KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations (English)
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    Marion Gaussen
    Vincent Meyer
    Laurent Orlando
    Batel Zimmerman
    Moriya Gamliel
    18 January 2012
    645-649

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