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Mosaicism of activatingFGFR3 mutations in human skin causes epidermal nevi
Epidermal nevi are common congenital skin lesions with an incidence of 1 in 1,000 people; however, their genetic basis remains elusive. Germline mutations of the FGF receptor 3 (FGFR3) cause autosomal dominant skeletal disorders such as achondroplasia and thanatophoric dysplasia, which can be associ...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society for Clinical Investigation
2006
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1501112/ https://ncbi.nlm.nih.gov/pubmed/16841094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI28163 |
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