Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)-Reference-Cited by-同舟云学术

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Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)

Published:1992-12 Issue:4 Volume:90 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Aldred MichaelJ.,Crawford PeterJ.M.,Roberts Enriqueta,Thomas NicholasS.T.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00220469.pdf

Cited by 99 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. AMELX Mutations and Genotype–Phenotype Correlation in X-Linked Amelogenesis Imperfecta;International Journal of Molecular Sciences;2024-06-01

2. Dental abnormalities in rare genetic bone diseases: Literature review;Clinical Anatomy;2023-09-22

3. Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4;Journal of Dental Research;2023-08-10

4. 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

5. The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta;Clinical Oral Investigations;2022-03-03

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