A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: clinical course and response to riboflavin

Overview of attention for article published in BMC Medical Genomics, May 2019

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Novel SLC52A2 #mutations https://t.co/A7xEv8IJ6H in #Chinese #patient with Brown-Vialetto-Van Laere syndrome #pediatrics progressive mental and motor regression and #drugresponse to #riboflavin https://t.co/jTJDb0ZwX6

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