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Cutaneous-Skeletal Hypophosphatemia Syndrome is a Multilineage Somatic Mosaic RASopathy
BACKGROUND: We recently demonstrated multilineage somatic mosaicism in cutaneous-skeletal hypophosphatemia syndrome (CSHS), which features epidermal or melanocytic nevi, elevated fibroblast growth factor-23 (FGF23) and hypophosphatemia, finding identical RAS mutations in affected skin and bone. OBJE...
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| 發表在: | J Am Acad Dermatol |
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| Main Authors: | , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5004488/ https://ncbi.nlm.nih.gov/pubmed/27444071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaad.2015.11.012 |
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