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Article

Five new homozygous mutations in the KIND1 gene in Kindler syndrome.

The Journal of investigative dermatology - 1 Sept 2007

Lai-Cheong Joey E, Liu Lu, Sethuraman Gomathy, Kumar Rajesh, Sharma Vinod K, Reddy Siva R, Vahlquist Anders, Pather Sandra, Arita Ken, Wessagowit Vesarat, McGrath John A

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PMID: 17460733
DOI: 10.1038/sj.jid.5700830

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Five new homozygous mutations in the KIND1 gene in Kindler syndrome.PMID 17460733Read ↗

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Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler SyndromeSemantic proximity Read ↗

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