Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population.
| Autor: | Yurong Piao1, Rongmin Li2, Yingjie Wang2, Congli Chen3, Yanmei Sang3 sangym_doc@126.com |
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| Zdroj: | Journal of Clinical Research in Pediatric Endocrinology. Dec2024, Vol. 16 Issue 4, p501-506. 6p. |
| Databáze: | Academic Search Ultimate |
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