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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.
Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
Epilepsia. 2015.
PMID: 26537434
Free article.
Transverse-momentum signatures for heavy Higgs bosons.
Cahn RN, Ellis SD, Kleiss R, Stirling WJ.
Cahn RN, et al. Among authors: kleiss r.
Phys Rev D Part Fields. 1987 Mar 1;35(5):1626-1632. doi: 10.1103/physrevd.35.1626.
Phys Rev D Part Fields. 1987.
PMID: 9957829
No abstract available.
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