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

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Bibliographic Details
Published in	British journal of dermatology (1951) Vol. 168; no. 2; pp. 456 - 458
Main Authors	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.
Format	Journal Article
Language	English
Published	01.02.2013
Online Access	Get full text

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ISSN:	0007-0963
DOI:	10.1111/j.1365-2133.2012.11181.x