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- W3149121036 abstract "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 reported in this paper." @default.
- W3149121036 created "2021-04-13" @default.
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- W3149121036 date "2021-04-01" @default.
- W3149121036 modified "2023-09-23" @default.
- W3149121036 title "[Basal cell nevus syndrome with Duchenne muscular dystrophy: a case report]." @default.
- W3149121036 doi "https://doi.org/10.7518/hxkq.2021.02.017" @default.
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