Literature DB >> 23466777

Dystrophic epidermolysis bullosa pruriginosa: the first report of a family in malaysia.

M M Tang1, K F Leong, H Cristina, L Bruckner-Tuderman.   

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Year:  2013        PMID： 23466777

Source DB:  PubMed          Journal:  Med J Malaysia        ISSN： 0300-5283


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  1 in total

1.  Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1.

Authors:  Pharuhad Pongmee; Sanchawan Wittayakornrerk; Ramrada Lekwuttikarn; Sasikarn Pakdeeto; Piangor Watcharakuldilok; Chatchay Prempunpong; Thipwimol Tim-Aroon; Chawintee Puttanapitak; Piyawan Wattanasoontornsakul; Thitiporn Junhasavasdikul; Parith Wongkittichote; Saisuda Noojarern; Duangrurdee Wattanasirichaigoon
Journal:  Front Genet       Date:  2022-04-01       Impact factor: 4.772
  1 in total

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