Expanding the Oro-Dental and Mutational Spectra of Kabuki Syndrome and Expression of KMT2D and KDM6A in Human Tooth Germs

Kabuki syndrome is a rare genetic disorder characterized by distinct dysmorphic facial features, intellectual disability, and multiple developmental abnormalities. Despite more than 350 documented cases, the oro-dental spectrum associated with kabuki syndrome and expression of KMT2D (histone-lysine...

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Detalles Bibliográficos
Autores principales: Porntaveetus, Thantrira, Abid, Mushriq F, Theerapanon, Thanakorn, Srichomthong, Chalurmpon, Ohazama, Atsushi, Kawasaki, Katsushige, Kawasaki, Maiko, Suphapeetiporn, Kanya, Sharpe, Paul T., Shotelersuk, Vorasuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930470/
https://www.ncbi.nlm.nih.gov/pubmed/29725259
http://dx.doi.org/10.7150/ijbs.23517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930470/
https://www.ncbi.nlm.nih.gov/pubmed/29725259
http://dx.doi.org/10.7150/ijbs.23517

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