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Several Mutations in the Melanocortin-4 Receptor Gene Including a Nonsense and a Frameshift Mutation Associated with Dominantly Inherited Obesity in Humans

机译：Melanocortin-4受体基因中的几种突变，包括废话和与人类中主要遗传肥胖相关的义义和框架突变

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A. Hinney; A. Schmidt; K. Nottebom; O. Heibült; I. Becker; A. Ziegler; G. Gerber; M. Sina; T. Görg; H. Mayer; W. Siegfried; M. Fichter; H. Remschmidt; J. Hebebrand;
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年度 1999
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1. A frameshift mutation in MC4R associated with dominantly inherited human obesity [J] . Yeo GSH., Aminian S., Halsall DJ., Nature Genetics . 1998,第2期

机译：MC4R移码突变与人类遗传性肥胖相关
2. Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms. [J] . Yeo GS, Lank EJ, Farooqi IS, Human Molecular Genetics . 2003,第5期

机译：与严重家族性肥胖症相关的人类黑皮质素4受体基因突变会通过多种分子机制破坏受体功能。
3. Autosomal-Dominant Mode of Inheritance of a Melanocortin-4 Receptor Mutation in a Patient with Severe Early-Onset Obesity Is Due to a Dominant-Negative Effect Caused by Receptor Dimerization. [J] . Gruters A Diabetes . 2003,第12期

机译：严重早期肥胖症患者中Melanocortin-4受体突变的遗传的常染色体显性模式是由于受体二聚作用引起的显性负作用。
4. Obesity-related mutations of leptin and melanocortin receptors [C] . Cecile Lubrano, Beatrice Dubern, Karine Clemen Colloque me?decine et recherche . 2006

机译：瘦素和黑素旋基因受体的肥胖相关突变
5. Targeted gene repair of frameshift mutations: Insights into the mechanism and applications for gene therapy [D] . Maguire, Katie K. 2007

机译：移码突变的靶向基因修复：深入了解基因治疗的机制和应用
6. Phenotypes in Three Pedigrees with Autosomal Dominant Obesity Caused by Haploinsufficiency Mutations in the Melanocortin-4 Receptor Gene [O] . Mani Sina, Anke Hinney, Andreas Ziegler, 1999

机译：导致常染色体显性肥胖的三个谱系的表型通过黑素皮质素4受体的单倍不足突变基因
7. Phenotypes in Three Pedigrees with Autosomal Dominant Obesity Caused by Haploinsufficiency Mutations in the Melanocortin-4 Receptor Gene [O] . Sina, Mani, Hinney, Anke, Ziegler, Andreas, 1999

机译：导致常染色体显性肥胖的三个谱系的表型通过黑素皮质素4受体的单倍不足突变基因

Several Mutations in the Melanocortin-4 Receptor Gene Including a Nonsense and a Frameshift Mutation Associated with Dominantly Inherited Obesity in Humans

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