Publishing research using ab116383? Please let us know so that we can cite the reference in this datasheet.

ab116383 has been referenced in 1 publication.

  • Wen J  et al. Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet J Rare Dis 8:100 (2013). WB . PubMed: 23837398

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"