Article info
PDFOriginal article
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)
- Correspondence to: Hatem El-Shanti University of Iowa Hospital, 2615 JCP, 200 Hawkins Drive, Iowa City, IA 52242, USA; hatem-el-shantiuiowa.edu
Citation
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)
Publication history
- Received January 5, 2005
- Accepted February 18, 2005
- Revised February 16, 2005
- First published July 1, 2005.
Online issue publication
April 27, 2016
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2005 Journal of Medical Genetics