Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants

Amelogenesis imperfecta (AI) refers to a genetically and clinically heterogeneous group of inherited disorders affecting the structure, composition, and quantity of tooth enamel. Both non-syndromic and syndromic forms of AI have been described and several genes affecting various aspects of the ename...

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Detalles Bibliográficos
Autores principales: Hytönen, Marjo K., Arumilli, Meharji, Sarkiala, Eva, Nieminen, Pekka, Lohi, Hannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536466/
https://www.ncbi.nlm.nih.gov/pubmed/30877375
http://dx.doi.org/10.1007/s00439-019-01997-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536466/
https://www.ncbi.nlm.nih.gov/pubmed/30877375
http://dx.doi.org/10.1007/s00439-019-01997-8

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