Table S1 - Phenotype-Genotype Correlation in Wilson Disease in a Large Lebanese Family: Association of c.2299insC with Hepatic and of p. Ala1003Thr with Neurologic Phenotype
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https://figshare.com/articles/dataset/_Phenotype_Genotype_Correlation_in_Wilson_Disease_in_a_Large_Lebanese_Family_Association_of_c_2299insC_with_Hepatic_and_of_p_Ala1003Thr_with_Neurologic_Phenotype_/1238660
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Normal (N) and mutant (M) nucleotide probes of mutations and SNPs identified in the S- Family in Exons: 8, 10, 12, 13, and 16. (DOCX)
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2015-12-02
