Title : [Clinical Characteristics and Gene Mutations in 186 Cases of Kindler Syndrome].

Pub. Date : 2022 Apr

PMID : 35538757






1 Functional Relationships(s)
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1 Conclusions The c.676C>T in FERMT1 gene is the most common mutation in KS.The patients are prone to squamous cell carcinoma and mainly attacked at the exposure sites(hand and mouth). Potassium FERM domain containing kindlin 1 Homo sapiens