Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli-Seip Congenital Lipodystrophy in a Cluster from Brazil-Reference-Cited by-同舟云学术

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Founder Effect of the 669insA Mutation in BSCL2 Gene Causing Berardinelli-Seip Congenital Lipodystrophy in a Cluster from Brazil

Published:2007-11 Issue:6 Volume:71 Page:729-734
ISSN:0003-4800
Container-title:Annals of Human Genetics
language:en
Short-container-title:Ann Human Genet

Author:

Gomes K. B.,Pardini V. C.,Ferreira A. C. S.,Fonseca C. G.,Fernandes A. P.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2007.00369.x/fullpdf

Reference24 articles.

1. AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34

2. Cardiomyopathy in congenital complete lipodystrophy

Cited by 3 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

A New Compound Heterozygous Mutation Of BSCL2 In A Chinese Zhuang Ethnic Family With Congenital Generalized Lipodystrophy

;Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy;2019-12

2. Lipodystrophy: pathophysiology and advances in treatment;Nature Reviews Endocrinology;2010-11-16

3. Clinical and molecular aspects of Berardinelli–Seip Congenital Lipodystrophy (BSCL);Clinica Chimica Acta;2009-04

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