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Clinical phenotype and CARD15 gene mutation with Blau Syndrome in Chinese children and their parents

Detalles Bibliográficos
Autores principales:	Li, C, He, X, Zhang, J, Han, T, Kuang, W
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2008
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334015/ http://dx.doi.org/10.1186/1546-0096-6-S1-P210

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