Literature DB >> 7539878

Birthmark due to cutaneous mosaicism for keratin 10 mutation.

C Moss, D O Jones, A Blight, P E Bowden.   

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Year:  1995        PMID： 7539878     DOI： 10.1016/s0140-6736(95)90510-3

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

Review 1.  Keratin gene mutations in disorders of human skin and its appendages.

Authors:  Jean Christopher Chamcheu; Imtiaz A Siddiqui; Deeba N Syed; Vaqar M Adhami; Mirjana Liovic; Hasan Mukhtar
Journal:  Arch Biochem Biophys       Date:  2010-12-19       Impact factor: 4.013

Review 2.  The molecular basis of human keratin disorders.

Authors:  Meral Julia Arin
Journal:  Hum Genet       Date:  2009-02-27       Impact factor: 4.132

3.  Bilateral Systematized Epidermolytic Verrucous Epidermal Nevus: A Rare Entity.

Authors:  Vivek Mishra; Abanti Saha; Debabrata Bandyopadhyay; Anirban Das
Journal:  Indian J Dermatol       Date:  2015 Jul-Aug       Impact factor: 1.494
  3 in total

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