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Spectrum of germline RB1 mutations and clinical manifestations in retinoblastoma patients from Thailand
PURPOSE: Retinoblastoma (RB) is a retinal tumor that most commonly occurs in children. Approximately 40% of RB patients carry germline mutations in the RB1 gene. RB survivors with germline mutations are at increased risk of passing on the disease to future offspring and of secondary cancer in adulth...
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| Vydáno v: | Mol Vis |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Molecular Vision
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6300611/ https://ncbi.nlm.nih.gov/pubmed/30636860 |
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