Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

By Weissenbach J.  

Human Molecular Genetics, Vol. 12, Iss. 18, 2003-09 ,pp. : 2369-2378

Oxford University Press

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger–Huët anomaly

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Human Molecular Genetics, Vol. 12, Iss. 1, 2003-01 ,pp. : 61-69

Oxford University Press

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Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis

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Human Molecular Genetics, Vol. 19, Iss. 13, 2010-07 ,pp. : 2594-2605

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Interleukin-1 alpha blockade prevents hyperkeratosis in an in vitro model of lamellar ichthyosis

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Human Molecular Genetics, Vol. 22, Iss. 5, 2013-03 ,pp. : 1059-1059

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