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基底细胞痣综合征伴杜氏肌营养不良症1例
Basal cell nevus syndrome (BCNS), also known as Gorlin-Goltz syndrome, is a rare autosomal dominant genetic disease. It is thought to be caused by a mutation in the PTCH1 gene, and its incidence is 1/57 000 to 1/256 000. The case of a 7-year-old patient with BCNS and Duchenne muscular dystrophy was...
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| Gepubliceerd in: | Hua Xi Kou Qiang Yi Xue Za Zhi |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
华西口腔医学杂志编辑部
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8055780/ https://ncbi.nlm.nih.gov/pubmed/33834681 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7518/hxkq.2021.02.017 |
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