SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/3/5/827/1701018/3-5-827.pdf
Cited by 68 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4;Journal of Dental Research;2023-08-10
2. An Intron c.103-3T>C Variant of the AMELX Gene Causes Combined Hypomineralized and Hypoplastic Type of Amelogenesis Imperfecta: Case Series and Review of the Literature;Genes;2022-07-18
3. Dose-Dependent Rescue of KO Amelogenin Enamel by Transgenes in Vivo;Frontiers in Physiology;2017-11-16
4. Deletion of Slc26a1 and Slc26a7 Delays Enamel Mineralization in Mice;Frontiers in Physiology;2017-05-16
5. MiR-153 Regulates Amelogenesis by Targeting Endocytotic and Endosomal/lysosomal Pathways–Novel Insight into the Origins of Enamel Pathologies;Scientific Reports;2017-03-13
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