檢索結果 - SG Mehta

  • Showing 1 - 2 results of 2
Refine Results
  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 由 GDJ Watts, Dana Thomasová, SK Ramdeen, Erin Fulchiero, SG Mehta, DA Drachman, C. Weihl, Zygmunt Jamrozik, Hubert Kwieciński, Anna Kamińska, VE Kimonis

    出版 2007
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 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

    出版 2012
    獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: