The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo. (Q40447118)

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The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo.
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    The Hsp60-(p.V98I) mutation associated with hereditary spastic paraplegia SPG13 compromises chaperonin function both in vitro and in vivo. (English)
    1 reference
    Peter Bross
    1 reference
    Søren Naundrup
    1 reference
    Jakob Hansen
    1 reference
    Marit Nyholm Nielsen
    1 reference
    Jane Hvarregaard Christensen
    1 reference
    Mogens Kruhøffer
    1 reference
    Johan Palmfeldt
    1 reference
    Niels Gregersen
    1 reference
    Debbie Ang
    1 reference
    Costa Georgopoulos
    1 reference
    Kåre Lehmann Nielsen
    1 reference
    8 April 2008
    1 reference
    283
    1 reference
    23
    1 reference
    15694-15700
    1 reference

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