Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.
作者:
主题词
青少年(Adolescent);成年人(Adult);发病年龄(Age of Onset);奥地利(Austria);儿童(Child);儿童, 学龄前(Child, Preschool);外显子(Exons);女(雌)性(Female);基因, 肾母细胞瘤(Genes, Wilms Tumor);德国(Germany);杂合子(Heterozygote);人类(Humans);婴儿(Infant);内含子(Introns);肾疾病(Kidney Diseases);肾肿瘤(Kidney Neoplasms);肾移植(Kidney Transplantation);男(雄)性(Male);突变, 误义(Mutation, Missense);肾切除术(Nephrectomy);表型(Phenotype);蛋白尿(Proteinuria);肾透析(Renal Dialysis);回顾性研究(Retrospective Studies);瑞士(Switzerland);泌尿生殖系统畸形(Urogenital Abnormalities);Wilms瘤(Wilms Tumor);青年人(Young Adult)
DOI
10.2215/CJN.10141014
PMID
25818337
发布时间
2018-11-13
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