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Paper Details

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.
Am J Hum Genet
249
2003
20p12, Caenorhabditis elegans, Caenorhabditis elegans actin-extracellular-matrix linker protein, Caenorhabditis elegans protein UNC-112, FLJ20116 gene, KIND1, KIND1", Kindler syndrome, Kindlin-1, UNC-112, abnormal pigmentation, actin, atrophy, autosomal recessive disorder, fragility of the skin, human, keratin, kindlin-1, neonatal blistering, skin fragility disorder

Datasets

Release 1.2