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

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Bibliographic Details
Published in:The Journal of clinical investigation 2005-04, Vol.115 (4), p.1100-1100
Main Authors: Ménasché, Gaël, Hsuan Ho, Chen, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, de Saint Basile, Geneviève
Format: Article
Language:English
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ISSN:0021-9738
DOI:10.1172/JCI18264C1