79 research outputs found

    Geometric multiaxial representation of N-qubit mixed symmetric separable states

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    Study of an N qubit mixed symmetric separable states is a long standing challenging problem as there exist no unique separability criterion. In this regard, we take up the N-qubit mixed symmetric separable states for a detailed study as these states are of experimental importance and offer elegant mathematical analysis since the dimension of the Hilbert space reduces from 2N to N + 1. Since there exists a one to one correspondence between spin-j system and an N-qubit symmetric state, we employ Fano statistical tensor parameters for the parametrization of spin density matrix. Further, we use geometric multiaxial representation (MAR) of density matrix to characterize the mixed symmetric separable states. Since separability problem is NP hard, we choose to study it in the continuum limit where mixed symmetric separable states are characterized by the P-distribution function λ (ᶿ, Φ) We show that the N-qubit mixed symmetric separable state can be visualized as a uniaxial system if the distribution function is independent of ᶿ, and Φ. We further choose distribution function to be the most general positive function on a sphere and observe that the statistical tensor parameters characterizing the N-qubit symmetric system are the expansion coefficients of the distribution function. As an example for the discrete case, we investigate the MAR of a uniformly weighted two qubit mixed symmetric separable state. We also observe that there exists a correspondence between separability and classicality of states

    De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

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    Variants in CLCN4, which encodes the chloride/hydrogen ion exchanger CIC-4 prominently expressed in brain, were recently described to cause X-linked intellectual disability and epilepsy. We present detailed phenotypic information on 52 individuals from 16 families with CLCN4-related disorder: 5 affected females and 2 affected males with a de novo variant in CLCN4 (6 individuals previously unreported) and 27 affected males, 3 affected females and 15 asymptomatic female carriers from 9 families with inherited CLCN4 variants (4 families previously unreported). Intellectual disability ranged from borderline to profound. Behavioral and psychiatric disorders were common in both child- and adulthood, and included autistic features, mood disorders, obsessive-compulsive behaviors and hetero- and autoaggression. Epilepsy was common, with severity ranging from epileptic encephalopathy to well-controlled seizures. Several affected individuals showed white matter changes on cerebral neuroimaging and progressive neurological symptoms, including movement disorders and spasticity. Heterozygous females can be as severely affected as males. The variability of symptoms in females is not correlated with the X inactivation pattern studied in their blood. The mutation spectrum includes frameshift, missense and splice site variants and one single-exon deletion. All missense variants were predicted to affect CLCN4's function based on in silico tools and either segregated with the phenotype in the family or were de novo. Pathogenicity of all previously unreported missense variants was further supported by electrophysiological studies in Xenopus laevis oocytes. We compare CLCN4-related disorder with conditions related to dysfunction of other members of the CLC family.E.E. Palmer ... E. Haan ... J. Nicholl, M. Shaw ... J. Gecz ... et al

    Papyrographic separation and location of antibiotics from plants

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