Genetic Diagnosis of Kindler Syndrome, a Rare form of Genodermatosis in a Newborn with Identification of a Nonsense Mutation, c. 328C > T, in the FERMT1 gene in the Indian population
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2. Loss of Kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome;Siegel;Am J Hum Genet,2003
3. Kindler syndrome;Lai-Cheong;Dermatol Clin,2010
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