Novel LAMB3 mutations cause non-syndromic amelogenesis imperfecta with variable expressivity

Detalles Bibliográficos
Autores principales: Lee, K-E, Ko, J, Le, CG Tran, Shin, TJ, Hyun, H-K, Lee, S-H, Kim, J-W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302247/
https://www.ncbi.nlm.nih.gov/pubmed/24494736
http://dx.doi.org/10.1111/cge.12340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302247/
https://www.ncbi.nlm.nih.gov/pubmed/24494736
http://dx.doi.org/10.1111/cge.12340

Ejemplares similares