학술논문 – 부산대학교 도서관

학술논문

replay검색결과 돌아가기

search검색화면

Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature

Document Type

Article

Author

Priestley, J.R.C.; Cuddapah, S.R.; Engelhardt, N.M.; Jolín García, P.C.; Ganetzky, R.D.; Pace, L.M.; Sen, K.; Gropman, A.; Aggarwal, A.; Alves, C.A.P.F.; Campbell, I.M.; Helbig, I.; Eskandar, M.; Lusk, L.; Hong, X.; Gowda, V.K.; Srinivasan, V.M.; Trapane, P.; Suwannarat, P.

Source

In: Molecular Genetics and Metabolism Reports. (Molecular Genetics and Metabolism Reports, December 2022, 33)

Subject

Language

English

ISSN

22144269

Online Access

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

이메일