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Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members

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Autores principales: Glanville, James, Taibjee, Saleem, Crow, Yanick, Davis, Penny, Ryder, Clive, Southwood, Taunton
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2011
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3194650/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1546-0096-9-S1-P283
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