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Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome.
Published in:
Journal of Investigative Dermatology, 2004, v. 122, n. 1, p. 78, doi. 10.1046/j.0022-202X.2003.22136.x
By:
- Ashton, Gabrielle H.S.;
- McLean, W.H. Irwin;
- South, Andrew P.;
- Oyama, Noritaka;
- Smith, Frances J.D.;
- Al-Suwaid, Raouf;
- Al Ismaily, Abla;
- Atherton, David J.;
- Harwood, Catherine A.;
- Leigh, Irene M.;
- Moss, Celia;
- Didona, Biagio;
- Zambruno, Giovanna;
- Patrizi, Annalisa;
- Eady, Robin A.J.;
- McGrath, John A.
Publication type:
Article
Extracellular Matrix Protein 1 Gene (ECM1 ) Mutations in Lipoid Proteinosis and Genotype-Phenotype Correlation.
Published in:
Journal of Investigative Dermatology, 2003, v. 120, n. 3, p. 345, doi. 10.1046/j.1523-1747.2003.12073.x
By:
- Hamada, Takahiro;
- Wessagowit, Vesarat;
- South, Andrew P.;
- Ashton, Gabrielle H.S.;
- Chan, Ien;
- Oyama, Noritaka;
- Siriwattana, Apatorn;
- Jewhasuchin, Prachiya;
- Charuwichitratana, Somyot;
- Thappa, Devinder M.;
- Lenane, Patsy;
- Krafchik, Bernice;
- Kulthanan, Kanokvalai;
- Shimizu, Hiroshi;
- Kaya, Tamer I.;
- Erdal, Mehmet E.;
- Paradisi, Mauro;
- Paller, Amy S.;
- Seishima, Mariko;
- Hashimoto, Takashi
Publication type:
Article