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Logo of jmedgeneJournal of Medical GeneticsVisit this articleSubmit a manuscriptReceive email alertsContact usBMJ
J Med Genet. 2007 June; 44(6): 407.
PMCID: PMC2740892


doi: 10.1136/jmg.2006.044644corr1

Jiao X, Sultana A, Garg P, Ramamurthy B, Vemuganti G K, Gangopadhyay N, Hejtmancik J F, Kannabiran C. Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11. J Med Genet 2007;44:64–8.

The journal apologises for an error that has occurred within this paper. In the abstract on page 64 (under Results, line 3) and in the key points box on page 67 (line 5) the term “limit of detection” should read as “LOD”.

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