Lv11
20 积分 2025-09-25 加入
Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion
1小时前
待审核
Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventions
1小时前
待审核
Hierarchically porous wood aerogel/polypyrrole(PPy) composite thick electrode for supercapacitor
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