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T. Hamada, W.H. McLean, M. Ramsay, G.H. Ashton i inni. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1). „Human Molecular Genetics”. 11 (7), s. 833–840, 2002. DOI: 10.1093/hmg/11.7.833. PMID: 11929856.
S. Di Giandomenico, R. Masi, D. Cassandrini, M. El-Hachem i inni. Lipoid proteinosis: case report and review of the literature. „Acta Otorhinolaryngologica Italica”. 26 (3), s. 162–167, 2006. PMID: 17063986.
M. Siebert, H.J. Markowitsch, P. Bartel. Amygdala, affect and cognition: evidence from 10 patients with Urbach-Wiethe disease. „Brain”. 126 (Pt 12), s. 2627–2637, 2003. DOI: 10.1093/brain/awg271. PMID: 12937075.