Overview of patients with SCN9A variants and their corresponding SCN1A mutation.
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https://figshare.com/articles/dataset/_Overview_of_patients_with_SCN9A_variants_and_their_corresponding_SCN1A_mutation_/553734
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*In Reference sequences used are: SCN9A (NP 002968) and SCN1A (Swiss-Prot P35498).AD, autosomal dominant; P, paternal; M, maternal; n.a., parents not available.
创建时间：
2015-12-02
