在诊断和减轻威尔逊病的纳米介导分子准

Akanksha Chaturvedi1, Swapnil Sharma2, Rahul Shukla3

  • 1Department of Pharmaceutics, National Institute of Pharmaceutical Education and Research-Raebareli (NIPER-Raebareli), Bijnor-Sisendi Road, Sarojini Nagar, Near CRPF Base Camp, Lucknow, UP, 226002, India.

Molecular neurobiology
|December 8, 2023
PubMed
概括

威尔逊病是一种由ATP7B基因突变引起的铜代谢遗传障碍,导致有毒铜的积累. 研究探索分子途径和纳米技术,以改善这种罕见疾病的诊断和治疗.