| 标题 |
专利、报告等 Whole exome sequencing of Nepalese siblings with Factor X Deficiency identifies an ultra-rare F10 p.F71S mutation: The first homozygous report outside Algeria |
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| DOI | |
| 其它 |
期刊:Springer Science and Business Media LLC 作者:Binod Neupane; Sridhar Sivasubbu; Tilak R. Shrestha 出版日期:2026-08-27 |
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(2025-6-4)