In recent years, significant progress has been made in the field of gene editing techniques, such as CRISPR-Cas9, allowing precise modifications of DNA to correct genetic defects. Furthermore, advancements in viral vector technologies have enabled more efficient and targeted delivery of therapeutic genes into patients' cells.
The Cell And Gene Therapy Market has witnessed a remarkable surge in...
Arabic
Français
Español
Português
Deutsch
Türkçe
Dutch
Italiano
Russian
Romaian