Type XV osteogenesis imperfecta: A novel mutation in the WNT1 gene, c.620G >A (p.R207H), is associated with an inner ear deformity
| Autor: | Jicai Zhu, Kai Liu, Shan He, Zihao Yang, Jiaying Song, Yan Ju, Caiyun Xiong, Guomei Zhang, Wen Yang, Chunhui Tang |
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| Rok vydání: | 2023 |
| Předmět: | |
| Zdroj: | Intractable & Rare Diseases Research. 12:58-61 |
| ISSN: | 2186-361X 2186-3644 |
| Databáze: | OpenAIRE |
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