Publishing research using ab38451? Please let us know so that we can cite the reference in this datasheet.

ab38451 has been referenced in 1 publication.

  • Akizu N  et al. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. Nat Genet 47:528-34 (2015). PubMed: 25848753

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