The 401 Project raises funds to conduct critical research to cure MECP2 Duplication Syndrome
“科学者たちは、MECP2重複症候群は可逆性疾患であると考えています。科学的研究を通して初めて可逆性は成し遂げられ、それには資金が必要です。私は、息子や息子と同疾患を抱えた世界中の子供たち、そしてその大切な子供たちの兄弟や両親のより良い生活を願い、この研究を可能とするための資金活動に全力を尽くします”
Recent research shows that there is great promise for curing MECP2 Duplication Syndrome. MECP2 Duplication Syndrome is a devastating neurological syndrome presenting first in infancy. Gene therapy research is advancing at exponential rates. Due to the straightforward genetic mutation causing MECP2 Duplication Syndrome, the syndrome is a first-line target for gene therapy.
Nearly all MECP2 Duplication Syndrome cure research has been funded by families and friends of children affected by MECP2 Duplication Syndrome.
Please join us in curing our children.
INFORMATION KIT NOW AVAILABLE CLICK IMAGE TO DOWNLOAD
About
Find out about our organization, mission, our methods, and the results of our years of advocacy.
Take Action
Ready to take the next step? You can become a contributor to our cause, or participate yourself.