Genetic Exclusion of 14 Candidate Genes in Lipoatropic Diabetes Using Linkage Analysis in 10 Consanguineous Families
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 30 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical and molecular aspects of Berardinelli–Seip Congenital Lipodystrophy (BSCL);Clinica Chimica Acta;2009-04
2. Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli-Seip Congenital Lipodystrophy in a Cluster from Brazil;Annals of Human Genetics;2007-11
3. Prevalence of Mutations in AGPAT2 Among Human Lipodystrophies;Diabetes;2003-06-01
4. Human Immunodeficiency Virus/Highly Active Antiretroviral Therapy-Associated Metabolic Syndrome: Clinical Presentation, Pathophysiology, and Therapeutic Strategies;The Journal of Clinical Endocrinology & Metabolism;2003-05
5. Lipoatrophic diabetes and other related syndromes;Reviews in Endocrine and Metabolic Disorders;2003
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