Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.
| Autor: | Jaebeen Kang1, Min-Ji Kim1, Sukdong Yoo1, Chong Kun Cheon1 chongkun@pusan.ac.kr |
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| Zdroj: | Annals of Pediatric Endocrinology & Metabolism. Jun2024, Vol. 29 Issue 3, p201-203. 3p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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