Rezultati pretrage - SG Mehta

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  1. 1
    Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

    Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia od GDJ Watts, Dana Thomasová, SK Ramdeen, Erin Fulchiero, SG Mehta, DA Drachman, C. Weihl, Zygmunt Jamrozik, Hubert Kwieciński, Anna Kamińska, VE Kimonis

    Izdano 2007
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  2. 2
    Genotype–phenotype studies of <scp>VCP</scp>‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

    Genotype–phenotype studies of <scp>VCP</scp>‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia od SG Mehta, Manaswitha Khare, R. Ramani, GDJ Watts, Mariella Simon, KE Osann, Sandra Donkervoort, Eric Dec, Angèle Nalbandian, Julia Platt, Marzia Pasquali, A Wang, Tahseen Mozaffar, CD Smith, VE Kimonis

    Izdano 2012
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