Clinical heterogeneity among a three-generation Japanese family with D18N TREX1 mutation for Aicardi-Goutières syndrome / familial chilblain lupus

Detalles Bibliográficos
Autores principales: Abe, J, Nishikomori, R, Izawa, K, Awaya, T, Kawai, T, Yasumi, T, Heike, T, Hiragi, N, Hiragi, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Poster Presentation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194642/
http://dx.doi.org/10.1186/1546-0096-9-S1-P276

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194642/
http://dx.doi.org/10.1186/1546-0096-9-S1-P276

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