Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
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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).(Ga?l Ménasché, Chen Hsuan)
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).(Ga?l Ménasché, Chen Hsuan)