While the industry hails progress in production, output remains hampered by several challenges as the clock ticks down to a key 2030 deadline.
While they are easing, plant closures and shifts towards electrified vehicles by manufacturers have also stunted the pace.Are electric cars really worth it? Here's Tom Heap's personal take.The SMMT has previously revealed research showing it could take five more years for a return to annual production of one million cars or more.
Those challenges are looming large in the mirror at a time when the clock is ticking in the UK to the 2030 ban on the sale of new cars powered by diesel and petrol.
Danmark Seneste Nyt, Danmark Overskrifter
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Campaigners criticise plans to boost housebuilding by relaxing environment rulesThe Government said the proposed change would allow for an additional 100,000 homes to be built in England by 2030.
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Campaigners criticise plans to boost housebuilding by relaxing environment rulesThe Government said the proposed change would allow for an additional 100,000 homes to be built in England by 2030.
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Team develops new fly model to find treatments for UBA5 deficiency, a rare epileptic brain disorderDevelopmental and epileptic encephalopathy (DEE) refers to a group of neurodevelopmental conditions characterized by developmental delay, cognitive impairment, and seizures in children. In 2016, the first case linking variants in both the copies of UBA5 gene to DEE44 was reported. Since then, twelve distinct missense variants in the UBA5 gene have been identified in 25 patients.
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Novel gene therapy significantly reduces hearing loss linked to rare disease in mouse modelAn international team led by researchers at UCL and the NIHR Great Ormond Street Hospital Biomedical Research Centre have developed in mice a gene therapy that significantly reduces the hearing loss associated with Norrie disease.
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Researchers develop new model to find potential treatment for neuromuscular diseasesResearchers from the Centre for Gene Therapy & Regenerative Medicine at King's College London, in collaboration with colleagues from University College London, have developed the first truly scalable human iPSC-neuromuscular disease model.
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