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A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis

Document Type

Article

Author

Grandin, V.; Lambert, N.; Picard, C.; de Saint Basile, G.; Sepulveda, F.E.; Ménasché, G.; Al Zahrani, M.; Al Idrissi, E.; Almanjomi, F.; K. Habazi, M.; A. Alghamdi, H.; Al-Mousa, H.; Al-Ghonaium, A.; Bole-Feysot, C.; Nitschke, P.

Source

In: Human Mutation. (Human Mutation, October 2017, 38(10):1355-1359)

Subject

Language

English

ISSN

10981004
10597794

Online Access

Full Text (Wiley Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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