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2. [Autoimmune blistering dermatoses in children].

3. Keratin-dependent thymic stromal lymphopoietin expression suggests a link between skin blistering and atopic disease.

4. A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases.

5. [The many facets of inherited skin fragility].

6. The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome.

7. Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination.

8. Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.

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