Publishing research using ab89181? Please let us know so that we can cite the reference in this datasheet.

ab89181 has been referenced in 1 publication.

  • Hardies K  et al. Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia. Brain 138:3238-50 (2015). PubMed: 26384929

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