| ［1］ |
Jobard F, Bouadjar B, Caux F, et al. Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome［J］. Hum Mol Genet, 2003,12（8）:925⁃935. doi: 10.1093/hmg/ddg097.
|
| ［2］ |
Suman N, Kaur S, Kaur S, et al. Kindler′s syndrome: a rare case report［J］. Contemp Clin Dent, 2014,5（2）:217⁃220. doi: 10. 4103/0976⁃237X.132342.
|
| ［3］ |
Barbosa NM, Visioli F, Martins MD, et al. Oral manifestations in Kindler syndrome: case report and discussion of literature findings［J］. Spec Care Dentist, 2016,36（4）:223⁃230. doi: 10. 1111/scd.12165.
|
| ［4］ |
El Hachem M, Diociaiuti A, Proto V, et al. Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree［J］. Eur J Dermatol, 2015,25（1）:14⁃19. doi: 10.1684/ejd.2014. 2457.
|
| ［5］ |
Souldi H, Bajja MY, Mahtar M. Kindler syndrome complicated by invasive squamous cell carcinoma of the palate［J］. Eur Ann Otorhinolaryngol Head Neck Dis, 2018,135（1）:59⁃61. doi: 10. 1016/j.anorl.2017.05.003.
|
| ［6］ |
Fischer IA, Kazandjieva J, Vassileva S, et al. Kindler syndrome: a case report and proposal for clinical diagnostic criteria［J］. Acta Dermatovenerol Alp Pannonica Adriat, 2005,14（2）:61⁃67.
|
| ［7］ |
林志淼, 谭燕红, 马志红, 等. 一例Kindler综合征患者皮损超微结构及FERMT1基因突变分析［J］. 中华皮肤科杂志, 2010,43（10）:677⁃679. doi: 10.3760/cma.j.issn.0412⁃4030.2010.10. 002.
|
| ［8］ |
Siegel DH, Ashton GH, Penagos HG, et al. Loss of kindlin⁃1, a human homolog of the Caenorhabditis elegans actin⁃extracellular⁃matrix linker protein UNC⁃112, causes Kindler syndrome［J］. Am J Hum Genet, 2003,73（1）:174⁃187. doi: 10.1086/376609.
|
| ［9］ |
Fuchs⁃Telem D, Nousbeck J, Singer A, et al. New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome［J］. Clin Exp Dermatol, 2014,39（3）:361⁃367. doi: 10.1111/ced.12222.
|
| ［10］ |
Has C, Castiglia D, del Rio M, et al. Kindler syndrome: extension of FERMT1 mutational spectrum and natural history［J］. Hum Mutat, 2011,32（11）:1204⁃1212. doi: 10.1002/humu.21576.
|
