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De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues

Document Type

Article

Author

Smits, D.J.; Schot, R.; Popescu, C.A.; Sleutels, F.J.G.T.; Mancini, G.M.S.; Dias, K.-R.; Roscioli, T.; Ades, L.; Briere, L.C.; Sweetser, D.A.; Kushima, I.; Aleksic, B.; Khan, S.; Karageorgou, V.; Ordonez, N.; Bertoli-Avella, A.M.; van der Kaay, D.C.M.; Van Mol, C.; Van Esch, H.

Source

In: Human Genetics. (Human Genetics, July 2023, 142(7):949-964)

Subject

Language

English

ISSN

14321203
03406717

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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