Glanville, J., Taibjee, S., Crow, Y., Davis, P., Ryder, C., & Southwood, T. (2011). Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with TREX1 mutation in 4 family members. BioMed Central.
Παραπομπή Chicago StyleGlanville, James, Saleem Taibjee, Yanick Crow, Penny Davis, Clive Ryder, και Taunton Southwood. Phenotypic Variation in Familial Chilblain Lupus (FCL) and Aicardi-Goutières Syndrome (AGS) Associated With TREX1 Mutation in 4 Family Members. BioMed Central, 2011.
Παραπομπή MLAGlanville, James, et al. Phenotypic Variation in Familial Chilblain Lupus (FCL) and Aicardi-Goutières Syndrome (AGS) Associated With TREX1 Mutation in 4 Family Members. BioMed Central, 2011.
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