2016, Number 1
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Dermatología Cosmética, Médica y Quirúrgica 2016; 14 (1)
The era of molecular diagnostics for hereditary skin diseases
Guajardo F, Salas AJC, Mcgrath J
Language: Spanish
References: 5
Page: 78-79
PDF size: 68.94 Kb.
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No abstract.
REFERENCES
Siañez-González C, Pezoa-Jares R, Salas-Alanis JC. “Congenital epidermolysis bullosa: a review”. Actas Dermosifiliogr 2009;100(10):842-856.
McGrath JA. “Rare inherited skin diseases and the Genomics England 100 000 Genome Project”. Br J Dermatol 2016;174(2):257-258.
Uitto J, Bruckner-Tuderman L, Christiano AM, et al. “Progress toward Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015”. J Invest Dermatol 2016;136(2):352-358.
Sathishkumar D, Orrin E, Terron-Kwiatkowski A, et al. “The p.Glu477Lys Mutation in Keratin 5 is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex”. J Invest Dermatol 2016;136(3):719-721.
McGrath JA. “Recently Identified Forms of Epidermolysis Bullosa”. Ann Dermatol 2015;27(6):658-666.
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