{"id":165275,"date":"2025-08-22T01:50:14","date_gmt":"2025-08-22T01:50:14","guid":{"rendered":"https:\/\/www.europesays.com\/us\/165275\/"},"modified":"2025-08-22T01:50:14","modified_gmt":"2025-08-22T01:50:14","slug":"a-japanese-familial-spastic-paraplegia-associated-with-a-missense-ubqln2-variant","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/us\/165275\/","title":{"rendered":"A Japanese familial spastic paraplegia associated with a missense UBQLN2 variant"},"content":{"rendered":"<li class=\"c-article-references__item js-c-reading-companion-references-item\" data-counter=\"1.\">\n<p class=\"c-article-references__text\" id=\"ref-CR1\">Statland JM, Barohn RJ, McVey AL, Katz JS, Dimachkie MM. Patterns of weakness, classification of motor neuron disease, and clinical diagnosis of sporadic amyotrophic lateral sclerosis. 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