Terahertz conductivity of the heavy-fermion compound UNi2Al3

We have studied the optical properties of the heavy-fermion compound UNi2Al3 at frequencies between 100 GHz and 1 THz (3 cm^-1 and 35 cm^-1), temperatures between 2 K and 300 K, and magnetic fields up to 7 T. From the measured transmission and phaseshift of radiation passing through a thin film of UNi2Al3, we have directly determined the frequency dependence of the real and imaginary parts of the optical conductivity (or permittivity, respectively). At low temperatures the anisotropy of the optical conductivity along the a- and c-axes is about 1.5. The frequency dependence of the real part of the optical conductivity shows a maximum at low temperatures, around 3 cm^-1 for the a-axis and around 4.5 cm^-1 for the c-axis. This feature is visible already at 30 K, much higher than the Neel temperature of 4.6 K, and it does not depend on external magnetic fields as high as 7 T. We conclude that this feature is independent of the antiferromagnetic order for UNi2Al3, and this might also be the case for UPd2Al3 and UPt3, where a similar maximum in the optical conductivity was observed previously.Comment: 7 pages, 9 figure

Observing the anisotropic optical response of the heavy-fermion compound UNi2Al3

The optical conductivity of heavy fermions can reveal fundamental properties of the charge carrier dynamics in these strongly correlated electron systems. Here we extend the conventional techniques of infrared optics on heavy fermions by measuring the transmission and phase shift of THz radiation that passes through a thin film of UNi2Al3, a material with hexagonal crystal structure. We deduce the optical conductivity in a previously not accessible frequency range, and furthermore we resolve the anisotropy of the optical response (parallel and perpendicular to the hexagonal planes). At frequencies around 7cm^-1, we find a strongly temperature-dependent and anisotropic optical conductivity that - surprisingly - roughly follows the dc behavior.Comment: 3 pages, 2 figures, accepted for proceedings of QCnP 200

Investigation of GRIN2A in common epilepsy phenotypes

Recently, mutations and deletions in the GRIN2A gene have been identified to predispose to benign and severe idiopathic focal epilepsies (IFE), revealing a higher incidence of GRIN2A alterations among the more severe phenotypes. This study aimed to explore the phenotypic boundaries of GRIN2A mutations by investigating patients with the two most common epilepsy syndromes: (i) idiopathic generalized epilepsy (IGE) and (ii) temporal lobe epilepsy (TLE). Whole exome sequencing data of 238 patients with IGE as well as Sanger sequencing of 84 patients with TLE were evaluated for GRIN2A sequence alterations. Two additional independent cohorts comprising 1469 IGE and 330 TLE patients were screened for structural deletions (>40. kb) involving GRIN2A. Apart from a presumably benign, non-segregating variant in a patient with juvenile absence epilepsy, neither mutations nor deletions were detected in either cohort. These findings suggest that mutations in GRIN2A preferentially are involved in genetic variance of pediatric IFE and do not contribute significantly to either adult focal epilepsies as TLE or generalized epilepsies