Additional file 3 of Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome
收藏Figshare2024-08-18 更新2026-04-08 收录
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https://springernature.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/26673354/1
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Additional file 3: Table S2. Phenotype–genotype correlations. Abbreviations: LoF, loss of function; OR, odds ratio; *, χ2 test.
提供机构：
Ramon y Cajal, Teresa; Robles, Luis; Teulé, Alexandre; Lázaro, Conxi; Dámaso, Estela; Berbel, Pere; Gómez, Luís; Sánchez-Mira, Andrea; Sevila, Carmen Martínez; Ibañez, Raquel Perea; Castillejo, Adela; Escandell, Inés; Soto, José Luis; Castillejo, M. Isabel; Sánchez-Martínez, Rosario; López-Fernández, Adrià; Balmaña, Judith; Robledo, Mercedes; Zúñiga, Ángel; Sánchez-Heras, Ana Beatriz
创建时间：
2024-08-14
