作者
Jan-Bernd Funcke, Julia von Schnurbein, Belinda Lennerz, Georgia Lahr, Klaus-Michael Debatin, Pamela Fischer-Posovszky, Martin Wabitsch
发表日期
2014/12
来源
Molecular and cellular pediatrics
卷号
1
页码范围
1-8
出版商
Springer Berlin Heidelberg
简介
Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight distinct mutations found so far in humans.
学术搜索中的文章
JB Funcke, J von Schnurbein, B Lennerz, G Lahr… - Molecular and cellular pediatrics, 2014