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Lucia Laugwitz1, Rebecca Buchert2, Patricio Olguín3

  • 1Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany; Neuropediatrics, General Paediatrics, Diabetology, Endocrinology and Social Paediatrics, University of Tübingen, University Hospital Tübingen, 72016 Tübingen, Germany.

概括

在EEFSEC的遗传变异导致由于蛋白缺乏导致罕见的神经退行性疾病. 这种先天性错误的类固醇代谢导致渐进的神经症状和小脑病理.

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