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. 2005 Apr 1;115(4):1100. doi: 10.1172/JCI200518264C1

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Gaël Ménasché, Chen Hsuan Ho, Ozden Sanal, Jérôme Feldmann, Ilhan Tezcan, Fügen Ersoy, Anne Houdusse, Alain Fischer, Geneviève de Saint Basile
PMCID: PMC1070401

Original citation: J. Clin. Invest. 112:450–456(2003). doi:10.1172/JCI200318264

Citation for this corrigendum: J. Clin. Invest. 115:1100 (2005). doi:10.1172/JCI200518264C1

During preparation of this manuscript for publication, an error was introduced into the first sentence of Methods regarding numbering of the 2 patients. The sentence should read:

The clinical presentation of patients A and B (PA and PB) has been previously reported (P13 and P12, respectively, in ref. 18).

The authors regret the error.


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