Literature DB >> 22672060

Case of Kindler syndrome resulting from mutation in the FERMT1 gene.

Makoto Wada, Koji Masuda, Daisuke Tsuruta, Katsuto Tamai, Joey E Lai-Cheong, John A McGrath, Norito Katoh.   

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Year:  2012        PMID： 22672060     DOI： 10.1111/j.1346-8138.2012.01598.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN： 0385-2407            Impact factor:   4.005


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  3 in total

1.  KIND1 Loss Sensitizes Keratinocytes to UV-Induced Inflammatory Response and DNA Damage.

Authors:  Xiaoling Zhang; Suju Luo; Joseph Wu; Long Zhang; Wen-Hui Wang; Simone Degan; Detlev Erdmann; Russell Hall; Jennifer Y Zhang
Journal:  J Invest Dermatol       Date:  2016-10-07       Impact factor: 8.551

2.  Ocular manifestations in Kindler syndrome.

Authors:  Prafulla K Maharana; Pranita Sahay; Sohini Mandal; Ritu Nagpal; Namrata Sharma
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

3.  Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.

Authors:  Susanne Krämer; James Lucas; Francisca Gamboa; Miguel Peñarrocha Diago; David Peñarrocha Oltra; Marcelo Guzmán-Letelier; Sanchit Paul; Gustavo Molina; Lorena Sepúlveda; Ignacio Araya; Rubén Soto; Carolina Arriagada; Anne W Lucky; Jemima E Mellerio; Roger Cornwall; Fatimah Alsayer; Reinhard Schilke; Mark Adam Antal; Fernanda Castrillón; Camila Paredes; Maria Concepción Serrano; Victoria Clark
Journal:  Spec Care Dentist       Date:  2020-11
  3 in total

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