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Full article: Autosomal dominant neovascular inflammatory vitreoretinopathy with CAPN5 c.731T > C gene mutation; clinical management of a family cohort and review of the literature
Emmanuel COUACY-HYMANN | Research Director and Head of Virology Laboratory | DMV, MSc, PhD, HDR | Virology Laboratory | Research profile
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Genes | Free Full-Text | Analysis of a Set of KDM5C Regulatory Genes Mutated in Neurodevelopmental Disorders Identifies Temporal Coexpression Brain Signatures
Nutrient intake and its possible drivers in free‐ranging European brown bears (Ursus arctos arctos) - De Cuyper - 2023 - Ecology and Evolution - Wiley Online Library
Motorový vůz řady 842 (M 273.2) | Atlas Lokomotiv
Frontiers | Complement Factor I Variants in Complement-Mediated Renal Diseases
Evolution of Brown Carbon Aerosols during Atmospheric Long-Range Transport in the South Asian Outflow and Himalayan Cryosphere | ACS Earth and Space Chemistry
Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration | PLOS Genetics
Panel testing for the molecular genetic diagnosis of congenital hypogonadotropic hypogonadism – a clinical perspective | European Journal of Human Genetics
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Generation and characterization of human iPSC lines derived from a Primary Hyperoxaluria Type I patient with p.I244T mutation - ScienceDirect
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Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium - ScienceDirect
Duration of SHIV production by infected cells is not exponentially distributed: Implications for estimates of infection parameters and antiviral efficacy | Scientific Reports
Low-Replicating Viruses and Strong Anti-Viral Immune Response Associated with Prolonged Disease Control in a Superinfected HIV-1 LTNP Elite Controller | PLOS ONE