Literature DB >> 25865288

A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome.

D Kartal1, M Borlu1, C Has2, R Fölster-Holst3.   

Abstract

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Year:  2015        PMID： 25865288     DOI： 10.1111/jdv.13163

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


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  4 in total

1.  A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.

Authors:  Ying Gao; Jin-li Bai; Xiao-yan Liu; Yu-jin Qu; Yan-yan Cao; Jian-cai Wang; Yu-wei Jin; Hong Wang; Fang Song
Journal:  J Zhejiang Univ Sci B       Date:  2015-11       Impact factor: 3.066

Review 2.  Novel Discoveries in Immune Dysregulation in Inborn Errors of Immunity.

Authors:  Anwen Ren; Wei Yin; Heather Miller; Lisa S Westerberg; Fabio Candotti; Chan-Sik Park; Pamela Lee; Quan Gong; Yan Chen; Chaohong Liu
Journal:  Front Immunol       Date:  2021-08-27       Impact factor: 7.561

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

4.  Kindler's Syndrome: A Tale of Two Siblings.

Authors:  Navya Handa; Dilip Kachhawa; Vinod Kumar Jain; Pankaj Rao; Anupam Das
Journal:  Indian J Dermatol       Date:  2016 Jul-Aug       Impact factor: 1.494
  4 in total

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