Literature DB >> 23083690

Lamellar ichthyosis due to ALOX12B mutation.

F Osório, M Leão, F Azevedo, S Magina.   

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Year:  2012        PMID： 23083690     DOI： 10.1016/j.ad.2012.07.011

Source DB:  PubMed          Journal:  Actas Dermosifiliogr        ISSN： 0001-7310


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  3 in total

1.  Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation.

Authors:  Sami Raja Alallasi; Amal A Kokandi; Babajan Banagnapali; Noor Ahmad Shaik; Bandar Ali Al-Shehri; Nuha Mohammad Alrayes; Jumana Yousuf Al-Aama; Musharraf Jelani
Journal:  Front Pediatr       Date:  2019-02-21       Impact factor: 3.418

2.  Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab.

Authors:  Faisal K Binkhonain; Sara Aldokhayel; Hessah BinJadeed; Abdulaziz Madani
Journal:  Biologics       Date:  2022-06-23

3.  Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy.

Authors:  Lei Zhang; Yanqiu Hu; Jingjing Lu; Peiwei Zhao; Xiankai Zhang; Li Tan; Jun Li; Cuiping Xiao; Linkong Zeng; Xuelian He
Journal:  Front Genet       Date:  2022-08-08       Impact factor: 4.772
  3 in total

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