| 标题 |
Identification of a novel intergenic EPCAM-MSH2 deletion causing EPCAM-associated Lynch syndrome by long-read nanopore sequencing |
| 网址 | |
| DOI |
10.1136/jmg-2026-111541
doi
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| 其它 |
期刊:Journal of Medical Genetics 作者:Luiza Steffens Reinhardt; Alexander Coster; Sean M. Burnard; Caitlin S. Romanis; Andrew Ziolkowski; et al 出版日期:2026-06-05 |
| 求助人 | |
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(2025-6-4)