Additional file 3 of Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome
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https://figshare.com/articles/dataset/Additional_file_3_of_Genetic_and_clinical_characterization_of_a_novel_FH_founder_mutation_in_families_with_hereditary_leiomyomatosis_and_renal_cell_cancer_syndrome/26673354
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Additional file 3: Table S2. Phenotype–genotype correlations. Abbreviations: LoF, loss of function; OR, odds ratio; *, χ2 test.
创建时间：
2024-01-26
