DNA based molecular analysis in the rapid diagnosis of Herlitz junctional epidermolysis bullosa
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2230.2001.00797.x/fullpdf
Reference9 articles.
1. Mutation analysis and molecular genetics of epidermolysis bullosa;Pulkkinen;Matrix Biol,1999
2. Hemidesmosomal variants of epidermolysis bullosa. Mutations in the alpha6 beta4 integrin and the 180-kD bullous pemphigoid antigen/type XVII collagen genes;Pulkkinen;Exp Dermatol,1998
3. Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa;McGrath;Nature Genet,1995
4. A homozygous nonsense mutation in the α3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa;Kivirikko;Hum Mol Genet,1995
5. A homozygous nonsense mutation in the β3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa;Pulkkinen;Genomics,1994
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1. 6 The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
2. The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
3. Síndrome de Bart asociado a epidermólisis ampollosa hereditaria letal (Herlitz);Actas Dermo-Sifiliográficas;2006-12
4. Paternal germline mosaicism in Herlitz junctional epidermolysis bullosa;Experimental Dermatology;2002-10
5. Soins infirmiers de l’épidermolyse bulleuse;Revue Française d'Allergologie et d'Immunologie Clinique;2001-11
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