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Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

Document Type

Article

Author

Luppe, J.; Lemke, J.R.; Abou Jamra, R.; Platzer, K.; Sticht, H.; Lecoquierre, F.; Goldenberg, A.; Gorman, K.M.; Molloy, B.; Agolini, E.; Novelli, A.; Briuglia, S.; Kuismin, O.; Marcelis, C.; Vitobello, A.; Denommé-Pichon, A.-S.; Julia, S.

Source

In: European Journal of Human Genetics. (European Journal of Human Genetics, March 2023, 31(3):345-352)

Subject

Language

English

ISSN

14765438
10184813

Online Access

Full Text (ProQuest Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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