Severe clinical phenotype caused by the <italic>COL4A5</italic> compound heterozygous variation in a female patient with X-linked dominant inheritance Alport syndrome： a case report and literature review
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| Main Author: | |
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| Format: | Article |
| Language: | zho |
| Published: |
Editorial Department of Journal of Clinical Nephrology
2025-05-01
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| Series: | Linchuang shenzangbing zazhi |
| Subjects: | |
| Online Access: | http://www.lcszb.com/thesisDetails#10.3969/j.issn.1671-2390.2025.05.015 |
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