Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.

Katja-Martina Eckl, Silvia de Juanes, Janine Kurtenbach, Marc Nätebus, Jenny Lugassy, Vinzenz Oji, Heiko Traupe, Marie-Luise Preil, Francisco Martínez, Josef Smolle, Avikam Harel, Peter Krieg, Eli Sprecher, Hans C Hennies

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