Publishing research using ab76786? Please let us know so that we can cite the reference in this datasheet.
ab76786 has been referenced in 3 publications.
Zhang M et al.A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China.Int J Clin Exp Pathol 8:5379-86 (2015).
Valente EM et al.Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.Nat Genet : (2010).
Romani S et al.The ciliary proteins Meckelin and Jouberin are required for retinoic acid-dependent neural differentiation of mouse embryonic stem cells.Differentiation 87:134-146 (0).
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