Publishing research using ab76786? Please let us know so that we can cite the reference in this datasheet.

ab76786 has been referenced in 1 publication.

  • Valente EM  et al. Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. Nat Genet : (2010). ICC/IF ; Human . PubMed: 20512146

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