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10 积分 2025-05-22 加入
Clinical and biochemical diagnostic and therapeutic survey of seven patients with lipid storage myopathy due to glutaric aciduria type II
1小时前
待确认
The clinical and genetical heterogeneity of riboflavin-responsive multiple acyl-coenzyme A dehydrogenase deficiency
3小时前
已完结
A late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition is more common in West of Scotland than primary genetic MADD, and is likely multifactorial
3小时前
已完结
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