4 results for author:"Oranje A.P." in Literature citations
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| The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron. van Steensel M.A., Oranje A.P., van der Schroeff J.G., Wagner A., van Geel M. Am. J. Med. Genet. A 149A:657-661(2009) · Mapped (1) |
| Development of atopic dermatitis in mice transgenic for human apolipoprotein C1. Nagelkerken L., Verzaal P., Lagerweij T., Persoon-Deen C., Berbee J.F., Prens E.P., Havekes L.M., Oranje A.P. J. Invest. Dermatol. 128:1165-1172(2008) · Mapped (2) |
| C-kit Asp-816-Val mutation analysis in patients with mastocytosis. Verzijl A., Heide R., Oranje A.P., van Schaik R.H. Dermatology (Basel) 214:15-20(2007) · Mapped (2) |
| Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1). Jonkman M.F., Moreno G., Rouan F., Oranje A.P., Pulkkinen L., Uitto J. J. Invest. Dermatol. 112:815-817(1999) · UniProtKB (1) |