首页> 美国卫生研究院文献>Diabetology Metabolic Syndrome >Leu124Serfs*26 a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications

【2h】

Leu124Serfs*26 a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications

机译：Leu124Serfs * 26先天性广义脂肪营养不良的新AGPAT2突变伴有早期心血管并发症

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

摘要
著录项
相似文献
相关主题

摘要

CGL pa–tients’ hometowns (in red) in the state of Ceará, Brazil

机译：巴西塞阿拉州CGL患者的家乡（红色）

著录项

期刊名称 Diabetology Metabolic Syndrome
作者
Renan Magalhães Montenegro Junior; Grayce Ellen da Cruz Paiva Lima; Virgínia Oliveira Fernandes; Ana Paula Dias Rangel Montenegro; Clarisse Mourão Melo Ponte; Lívia Vasconcelos Martins; Daniel Pascoalino Pinheiro; Maria Elisabete Amaral de Moraes; Manoel Odorico de Moraes Filho; Catarina Brasil d’Alva;
展开▼
作者单位

展开▼
年(卷),期 2020(12),-1
年度 2020
页码 -1
总页数 9
原文格式 PDF
正文语种
中图分类基础医学;
关键词
Congenital generalized lipodystrophy;

机译：先天性全身脂肪营养不良;

相似文献

外文文献
中文文献
专利

1. Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli-Seip congenital generalized lipodystrophy syndrome. [J] . Miranda DM, Wajchenberg BL, Calsolari MR Clinical Endocrinology . 2009,第4期

机译：患有Berardinelli-Seip先天性全身性脂肪营养不良综合征的10个家庭的BSCL2和AGPAT2基因的新型突变。
2. A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy [J] . Clinical Endocrinology . 2020,第2期

机译：来自Gaza的AgPat2基因中的罕见帧突变突变，具有先天性广义唇脂
3. A novel variant of the AGPAT2 mutation in generalized congenital lipodystrophy [J] . Sahana Shetty, Aaron Chapla, Nitin Kapoor, Australasian Medical Journal . 2016,第6期

机译：广泛性先天性脂肪营养不良的AGPAT2突变的新型变体
4. Nursing Intervention to Prevent Complications in Children with Congenital Heart Disease after Operation Vomiting [C] . Bo Ma, Dongxue Shen, He Liang, International Symposium on Biomedical Science, Biotechnology and Healthcare . 2018

机译：护理干预以防止在术后先天性心脏病儿童的并发症
5. Molecular analysis of PPARgamma mutations associated with diabetes and lipodystrophy. [D] . Li, Gang. 2006

机译：与糖尿病和脂肪营养不良有关的PPARγ突变的分子分析。
6. Divergent Metabolic Phenotype between Two Sisters with Congenital Generalized Lipodystrophy Due to Double AGPAT2 Homozygous Mutations. A Clinical Genetic and In Silico Study [O] . Víctor A. Cortés, Susan V. Smalley, Denisse Goldenberg, -1

机译：由于双AGPAT2纯合突变先天性全身脂肪营养不良的两个姐妹之间的分歧代谢表型。临床遗传和计算机模拟研究
7. Divergent metabolic phenotype between two sisters with congenital generalized lipodystrophy due to double AGPAT2 homozygous mutations. a clinical, genetic and in silico study. [O] . Víctor A Cortés, Susan V Smalley, Denisse Goldenberg, 2014

机译：由于双重aGpaT2纯合突变导致先天性全身性脂肪代谢障碍的两姐妹之间的代谢表型不同。临床，遗传和计算机研究。

Leu124Serfs*26 a novel AGPAT2 mutation in congenital generalized lipodystrophy with early cardiovascular complications

摘要

著录项

相似文献

相关主题

期刊订阅