Publishing research using ab56984? Please let us know so that we can cite the reference in this datasheet.
ab56984 has been referenced in 1 publication.
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).
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