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).
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).
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Get resources and offers direct to your inboxSign up