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机译:用H综合征在两个不同的叙利亚家族中编码平衡核苷转运蛋白(HENT3)的SLC29a3中的两种新突变:SLC29A3(HENT3)在人体皮肤中的表达研究
Laboratory of Genetic Skin Diseases Niigata University Graduate School of Medical and Dental;
Department of Dermatology and Venereology University Hospital Damascus Syrian Arab Republic;
Laboratory of Genetic Skin Diseases Niigata University Graduate School of Medical and Dental;
Laboratory of Genetic Skin Diseases Niigata University Graduate School of Medical and Dental;
Departments of Dermatology Beirut Lebanon;
Departments of Dermatology Beirut Lebanon;
Departments of Dermatology Beirut Lebanon Biochemistry and Molecular Genetics American;
Laboratory of Genetic Skin Diseases Niigata University Graduate School of Medical and Dental;
H syndrome; Histiocytes; Hyperpigmentation; Hypertrichosis; SLC29A3;
机译:SLC29A3中两个新的突变的鉴定,该突变在两个具有H综合征的叙利亚不同家庭中编码一个平衡核苷转运蛋白(hENT3):SLC29A3(hENT3)在人皮肤中的表达研究
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机译:双嘧达莫和draflazine类似物作为人类平衡核苷转运蛋白hENT1和hENT2抑制剂的研究。
机译:SLC29A3中的突变编码一个平衡的核苷转运蛋白ENT3导致家族性组织细胞增多症(Faisalabad组织细胞增多症)和家族性Rosai-Dorfman病
机译:SLC29A3中的突变,编码一个平衡的核苷转运蛋白ENT3,导致家族性组织细胞增多症(Faisalabad组织细胞增多症)和家族性Rosai-Dorfman病