Lv3
210 积分 2024-06-23 加入
A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia
7小时前
已完结
20-Year Follow-up of Statins in Children with Familial Hypercholesterolemia
9小时前
已完结
[Phenotypes and ATP7B gene variants in 316 children with Wilson disease]
23天前
已完结
Molecular genetics of the LDL receptor gene in familial hypercholesterolemia
1个月前
已完结
Interpretation of mitochondrial tRNA variants
1个月前
已完结
Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)
1个月前
已完结
Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease
2个月前
已关闭
Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance
2个月前
已完结
Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis
3个月前
已完结
A Mutation in the Vesicle-Trafficking Protein VAPB Causes Late-Onset Spinal Muscular Atrophy and Amyotrophic Lateral Sclerosis
3个月前
已完结
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