发表研究结果有使用 ab76786?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab76786 被引用在 1 文献中.

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

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