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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

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