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Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome
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| 發表在: | Ann Dermatol |
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| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Korean Dermatological Association; The Korean Society for Investigative Dermatology
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4969485/ https://ncbi.nlm.nih.gov/pubmed/27489438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5021/ad.2016.28.4.503 |
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