Loss of Kindlin-1 Causes Skin Atrophy and Lethal Neonatal Intestinal Epithelial Dysfunction

Kindler Syndrome (KS), characterized by transient skin blistering followed by abnormal pigmentation, skin atrophy, and skin cancer, is caused by mutations in the FERMT1 gene. Although a few KS patients have been reported to also develop ulcerative colitis (UC), a causal link to the FERMT1 gene mutat...

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Main Authors: Ussar, Siegfried, Moser, Markus, Widmaier, Moritz, Rognoni, Emanuel, Harrer, Christian, Genzel-Boroviczeny, Orsolya, Fässler, Reinhard
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2008
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2585060/
https://ncbi.nlm.nih.gov/pubmed/19057668
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000289
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