A severe familial phenotype of Ichthyosis Curth-Macklin...

British Journal of Dermatology 2013 / 02 Vol. 168; Iss. 2

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

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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Volume:
168
Language:
english
Journal:
British Journal of Dermatology
DOI:
10.1111/j.1365-2133.2012.11181.x
Date:
February, 2013
File:
PDF, 515 KB
english, 2013
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