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Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

Document Type

Article

Author

Ismail, V.; Foulds, N.; Baralle, D.; Zachariassen, L.G.; Sahakian, M.; Lyngby, S.M.; Pedersen, M.G.; Kristensen, A.S.; Wheway, G.; Godwin, A.; Guille, M.; Ellard, S.; Stals, K.L.; Baple, E.; Brown, K.T.; Parker, M.O.; Desir, J.; Bayat, A.; Musgaard, M.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 7 July 2022, 109(7):1217-1241)

Subject

Language

English

ISSN

15376605
00029297

Online Access

Full Text (ScienceDirect 종량제) Open Access (EBSCO) Full Text (ScienceDirect O/A) Web of Science JCR 저널정보 Scopus Find it@PNU

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