Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

The identification of causative genetic variants for hereditary diseases has revolutionized clinical medicine and an extensive collaborative framework with international cooperation has become a global trend to understand rare disorders. The Initiative on Rare and Undiagnosed Diseases (IRUD) was est...

Descripción completa

Detalles Bibliográficos
Autores principales: Takahashi, Yuji, Date, Hidetoshi, Oi, Hideki, Adachi, Takeya, Imanishi, Noriaki, Kimura, En, Takizawa, Hotake, Kosugi, Shinji, Matsumoto, Naomichi, Kosaki, Kenjiro, Matsubara, Yoichi, Mizusawa, Hidehiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402437/
https://www.ncbi.nlm.nih.gov/pubmed/35318459
http://dx.doi.org/10.1038/s10038-022-01025-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9402437/
https://www.ncbi.nlm.nih.gov/pubmed/35318459
http://dx.doi.org/10.1038/s10038-022-01025-0

Ejemplares similares