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Klippel–Trenaunay and Sturge–Weber Overlap Syndrome with KRAS and GNAQ mutations
Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated. We reported the patient presenting with Klippel–Trenaunay and Sturge–Weber overlap syndrome in mainland...
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| 出版年: | Ann Clin Transl Neurol |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2020
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7359123/ https://ncbi.nlm.nih.gov/pubmed/32613723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51106 |
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