OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation (Q30494366)

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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation
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    OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation (English)
    1 reference
    Tadato Ban
    1 reference
    Jürgen A W Heymann
    1 reference
    Zhiyin Song
    1 reference
    Jenny E Hinshaw
    1 reference
    David C Chan
    1 reference
    25 February 2010
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    19
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    2113-2122
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    11
    1 reference

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