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Griscelli syndrome without hemophagocytosis in an eleven-year-old girl: Expanding the phenotypic spectrum of Rab27A mutations in humans

✍ Scribed by Güzide Aksu; Necil Kütükçüler; Ferah Genel; Canan Vergin; Benjamin Omowaire


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
64 KB
Volume
116A
Category
Article
ISSN
1552-4825

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