Detailed assessment of rare and common TERT variation in a family with a telomere biology disorder
Summary: Telomere biology disorders (TBDs) are caused by rare pathogenic variants in telomere maintenance genes and often present with variable penetrance of multi-organ system manifestations. We evaluated a family with 14 individuals heterozygous for TERT c.2591T>C (p.L864P) and 13 non-carriers. TR...
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2026-01-01
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| Edice: | HGG Advances |
| Témata: | |
| On-line přístup: | http://www.sciencedirect.com/science/article/pii/S2666247725001393 |
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