Literature DB >> 27520397

Identification of a novel mutation in the LOR gene in an Iraqi patient with loricrin keratoderma resembling epidermolytic hyperkeratosis.

S Khalil1, L Daou1, R Hayashi2, O Abbas3, G Nemer4, D Saadeh3, Y Shimomura2,5, M Kurban3,4,6.   

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Year:  2016        PMID： 27520397     DOI： 10.1111/jdv.13882

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


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  1 in total

1.  Somatic recombination underlies frequent revertant mosaicism in loricrin keratoderma.

Authors:  Shotaro Suzuki; Toshifumi Nomura; Toshinari Miyauchi; Masae Takeda; Yasuyuki Fujita; Wataru Nishie; Masashi Akiyama; Akemi Ishida-Yamamoto; Hiroshi Shimizu
Journal:  Life Sci Alliance       Date:  2019-02-04
  1 in total

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