Hundreds of seriously ill patients in the UK suffering from undiagnosed conditions have had the underlying genetic causes pinpointed by a groundbreaking project, which scientists believe will cut the cost to the NHS of treating rare diseases and improve patient care.
英国一项开创性的项目找到了数百名患有未确诊疾病的重症患者的潜在遗传原因。科学家们相信，该项目将降低英国国民医疗服务体系(NHS)治疗罕见疾病的成本，并改善患者护理。
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