Publishing research using ab56984? Please let us know so that we can cite the reference in this datasheet.

ab56984 has been referenced in 2 publications.

  • Roda RH  et al. Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage. J Clin Neurosci 21:1627-31 (2014). PubMed: 24814856
  • Nanetti L  et al. SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet J Rare Dis 8:123 (2013). WB ; Human . PubMed: 23941260

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