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).
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