发表研究结果有使用 ab92950?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab92950 被引用在 1 文献中.

  • Logan CV  et al. Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII a1 Chain. Am J Hum Genet 97:878-85 (2015). PubMed: 26626625

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