IIIB 型粘多糖病: AAV 疗法的现状回顾和探索
CJ Rouse, VN Jensen, CD Heldermon - 中国神经再生研究(英文版), 2024 - sjzsyj.com.cn
Mucopolysaccharidoses type IIIB is a rare genetic disorder caused by mutations in the gene
that encodes for N-acetyl-alpha-glucosaminidase. This results in the aggregation of heparan …
that encodes for N-acetyl-alpha-glucosaminidase. This results in the aggregation of heparan …
IIIB 型粘多糖病: AAV 疗法的现状回顾和探索
CJ Rouse, VN Jensen, CD Heldermon - 中国神经再生研究(英文版), 2024 - sjzsyj.com.cn
Mucopolysaccharidoses type IIIB is a rare genetic disorder caused by mutations in the gene
that encodes for N-acetyl-alpha-glucosaminidase. This results in the aggregation of heparan …
that encodes for N-acetyl-alpha-glucosaminidase. This results in the aggregation of heparan …