Subject
Dermatology,Pediatrics, Perinatology and Child Health
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3. Loss of kindling-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome;Siegel;Am J Hum Genet,2003
4. Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome;Ashton;J Invest Dermatol,2004
5. Kindler syndrome: a case report and proposal for clinical diagnostic criteria;Angelova-Fischer;Acta Dermatovenerol Alp Panonica Adriat,2005
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