| 1 | KHM1, LOR
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| Activation of vascular endothelial growth factor receptor 2 in a cellular model of loricrin keratoderma.
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| Yoneda K, Demitsu T, Nakai K, Moriue T, Ogawa W, Igarashi J, Kosaka H, Kubota Y.
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| J Biol Chem 285(21):16184-94. Epub 2010 Mar 17.
2010
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| 2 | KHM1, LOR
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| Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby.
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| Matsumoto K, Muto M, Seki S, Saida T, Horiuchi N, Takahashi H, Ishida-Yamamoto A, Iizuka H.
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| Br J Dermatol 145(4):657-60.
2001
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| 3 | KHM1, LOR
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| Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis.
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| Korge BP, Ishida-Yamamoto A, Punter C, Dopping-Hepenstal PJ, Iizuka H, Stephenson A, Eady RA, Munro CS.
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| J Invest Dermatol 109(4):604-10. 1997
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| 4 | LOR, KHM1
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| A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome.
|
| Maestrini E, et al.
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| Nat Genet 13 : 70-77. 1996
|