Computational approach towards identification of pathogenic missense mutations in AMELX gene and their possible association with amelogenesis imperfecta

Amelogenin gene (AMEL-X) encodes an enamel protein called amelogenin, which plays a vital role in tooth development. Any mutations in this gene or the associated pathway lead to developmental abnormalities of the tooth. The present study aims to analyze functional missense mutations in AMEL-X genes...

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Detalles Bibliográficos
Autores principales: Shivani, Narendra, Smiline-Girija, Aseervatham Selvi, Paramasivam, Arumugam, Vijayashree-Priyadharsini, Jayaseelan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382399/
https://www.ncbi.nlm.nih.gov/pubmed/32802900
http://dx.doi.org/10.22099/mbrc.2020.35413.1456

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382399/
https://www.ncbi.nlm.nih.gov/pubmed/32802900
http://dx.doi.org/10.22099/mbrc.2020.35413.1456

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