Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho‐dento‐osseous syndrome

OBJECTIVES: Variants in DLX3 cause tricho‐dento‐osseous syndrome (TDO, MIM #190320), a systemic condition with hair, nail and bony changes, taurodontism and amelogenesis imperfecta (AI), inherited in an autosomal dominant fashion. Different variants found within this gene are associated with differe...

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Detalles Bibliográficos
Autores principales: Whitehouse, Laura L. E., Smith, Claire E. L., Poulter, James A., Brown, Catriona J., Patel, Anesha, Lamb, Teresa, Brown, Lucy R., O’Sullivan, Elizabeth A., Mitchell, Rowena E., Berry, Ian R., Charlton, Ruth, Inglehearn, Chris F., Mighell, Alan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Bone and Hard Tissues
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334507/
https://www.ncbi.nlm.nih.gov/pubmed/30095208
http://dx.doi.org/10.1111/odi.12955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334507/
https://www.ncbi.nlm.nih.gov/pubmed/30095208
http://dx.doi.org/10.1111/odi.12955

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