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.
استشهاد بنمط شيكاغوGlanville, James, Saleem Taibjee, Yanick Crow, Penny Davis, Clive Ryder, و 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.
MLA استشهادGlanville, 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.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.