机译:DHTKD1突变导致2-氨辅助纤维和2-氧晚酸核
Institute of Human Genetics Technische Universit?t München 81675 Munich Germany Institute of;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
Institute of Human Genetics Technische Universit?t München 81675 Munich Germany Institute of;
Institute of Human Genetics Helmholtz Zentrum München German Research Center for Environmental;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
Institute of Human Genetics Helmholtz Zentrum München German Research Center for Environmental;
Division of Human Genetics Medical University Innsbruck 6020 Innsbruck Austria;
Institute of Human Genetics Technische Universit?t München 81675 Munich Germany Institute of;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
Institute of Human Genetics Technische Universit?t München 81675 Munich Germany Institute of;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
Institute of Human Genetics Technische Universit?t München 81675 Munich Germany Institute of;
Department of General Pediatrics Division of Inherited Metabolic Diseases University Children's;
机译:DHTKD1突变导致2-氨基己二酸和2-氧己二酸尿症
机译:Kearns-Sayre综合征表现为2-氧己二酸尿症。
机译:2-氧己二酸尿症的犬尿氨酸正常代谢。
机译:衰老,糖尿病和肾功能衰竭催化赖氨酸残基的氧化在人体皮肤胶原蛋白中的2-氨基甲酸
机译:具有肿瘤特异性高通量体细胞突变(CHASM)的肿瘤测序研究中检测到的体细胞错义突变的计算评估。
机译:DHTKD1突变导致2-氨基己二酸和2-氧己二酸尿症
机译:DHTKD1突变导致2-氨基己二酸和2-氧己二酸尿症
机译:msUD(枫糖浆尿病)和有机酸尿症的饮食疗法