논문KCI 등재
Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
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참고문헌 (5)
- Lai-Cheong JE., "Kindler syndrome : a focal adhesion genodermatosis", Br J Dermatol, 160, pp.233~242 (2009)
- Rognoni E., "Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation", Nat Med, 20, pp.350~359 (2014)
- Has C., "Kindler syndrome : extension of FERMT1 mutational spectrum and natural history", Hum Mutat, 32, pp.1204~1212 (2011)
- Youssefian L., "The Kindler syndrome : a spectrum of FERMT1 mutations in Iranian families", J Invest Dermatol, 135, pp.1447~1450 (2015)
- Ohashi A., "A case of Kindler syndrome with severe esophageal stenosis", Int J Dermatol, 54, pp.e106~e108 (2015)
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