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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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)
创建时间：
2015-12-02
