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  • Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)

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Original article
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)
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Authors

  1. Correspondence to:
 Hatem El-Shanti
 University of Iowa Hospital, 2615 JCP, 200 Hawkins Drive, Iowa City, IA 52242, USA; hatem-el-shantiuiowa.edu
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Citation

Ferguson PJ, Chen S, Tayeh MK, et al
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)
Journal of Medical Genetics 2005;42:551-557.

Publication history

  • Received January 5, 2005
  • Accepted February 18, 2005
  • Revised February 16, 2005
  • First published July 1, 2005.
Online issue publication 
July 01, 2005

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    Files in this Data Supplement:

    • [view PDF] - Table: LPIN2 primer sequence, amplification size, and annealing temperature.

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Copyright 2005 Journal of Medical Genetics