Publishing research using ab122879? Please let us know so that we can cite the reference in this datasheet.

ab122879 has been referenced in 1 publication.

  • Halbritter J  et al. Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. Am J Hum Genet 93:915-25 (2013). Human . PubMed: 24140113

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