Literature DB >> 14962094

A novel nonsense mutation in Kindler syndrome.

Cristina Has, Leena Bruckner-Tuderman.   

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Year:  2004        PMID： 14962094     DOI： 10.1046/j.0022-202X.2003.22138.x

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  2 in total

1.  Loss-of-function FERMT1 mutations in kindler syndrome implicate a role for fermitin family homolog-1 in integrin activation.

Authors:  Joey E Lai-Cheong; Maddy Parsons; Akio Tanaka; Siegfried Ussar; Andrew P South; Sethuraman Gomathy; John B Mee; Jean-Baptiste Barbaroux; Tanasit Techanukul; Noor Almaani; Suzanne E Clements; Ian R Hart; John A McGrath
Journal:  Am J Pathol       Date:  2009-09-17       Impact factor: 4.307

Review 2.  [Hereditary blistering disorders].

Authors:  C Has; J S Kern; L Bruckner-Tuderman
Journal:  Hautarzt       Date:  2004-10       Impact factor: 0.751
  2 in total

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