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A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene

✍ Scribed by Fonseca, D.J.; Rojas, R.F.; Vergara, J.I.; Ríos, X.; Uribe, C.; Chávez, L.; Velandia, F.; Vargas, C.I.; Restrepo, C.M.; Laissue, P.

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