A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases
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| Veröffentlicht in: | Journal of dermatological science 2016, Vol.82 (2), p.134-137 |
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| Sprache: | eng |
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| container_end_page | 137 |
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| container_issue | 2 |
| container_start_page | 134 |
| container_title | Journal of dermatological science |
| container_volume | 82 |
| creator | Teye, Kwesi Suga, Yasushi Numata, Sanae Soejima, Mikiko Ishii, Norito Krol, Rafal P Ohata, Chika Matsuda, Mitsuhiro Honma, Masaru Ishida-Yamamoto, Akemi Hamada, Takahiro Koda, Yoshiro Hashimoto, Takashi |
| description | |
| doi_str_mv | 10.1016/j.jdermsci.2016.01.012 |
| format | Report |
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| fulltext | fulltext |
| identifier | EISSN: 1873-569X |
| ispartof | Journal of dermatological science, 2016, Vol.82 (2), p.134-137 |
| issn | 1873-569X |
| language | eng |
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| source | Elsevier ScienceDirect Journals Complete |
| title | A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases |
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