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Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome

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書目詳細資料
發表在:Ann Dermatol
Main Authors: Oh, Seung Joon, Kim, Song-Ee, Lee, Sang Eun, Kim, Soo-Chan
格式: Artigo
語言:Inglês
出版: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2016
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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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