Zanini M, Bertino D, Corrêa e Silva K, Camargo PLH, Landaman G, Freitas E

Idioma: Portugués
Referencias bibliográficas: 14
Paginas: 192-194
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RESUMEN

Sin resumen.

REFERENCIAS (EN ESTE ARTÍCULO)

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9. Ishida-Yamamoto A, McGrath JA, Lam H, Iizuka H, Friedman RA, Christiano AM. The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope. Am J Hum Genet 1997; 61:581-9.

10. Suga Y; Jarnik M; Attar PS et al. Transgenic mice expressing a mutant form of loricrin reveal the molecular basis of the skin diseases, Vohwinkel syndrome and progressive symmetric erythrokeratoderma. J Cell Biol 2000; 151:401-12.

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