Table S1 - Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation
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https://figshare.com/articles/dataset/Molecular_and_Clinical_Characterization_of_the_Variable_Phenotype_in_Korean_Families_with_Hearing_Loss_Associated_with_the_Mitochondrial_A1555G_Mutation/121660
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Primer sequences used for whole mtDNA genome analysis. Bold sequences denote primers using PCR. Sequences of the rest are used for internal sequence primers. (DOC)
创建时间：
2015-12-02
