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Register with us to receive latest news & updates related to ASH1L. If there is a new research or a new paper published then you will be notified by an email in your registered email address. This way you can stay up-to-date with all the latest developments on ASH1L. 

You can also join us on our Facebook group or contact us

Help us in creating and raising awareness about the disorders related to ASH1L gene mutation. Diagnosing ASH1L requires intrinsic genetic tests that most often are not recommended by doctors. ASH1L is a critical gene that is shown to affect other genes thereby causing complicated health conditions. Help us reach out to doctors, medical professionals, researchers, scientists, universities, pharmaceutical companies and also raise funds for scientific research. 

Help us support our cause - 

  • Increase awareness about ASH1L

  • Encourage future collaborations with scientists, researchers and/or universities to deepen the ASH1L study by using animal models or other therapeutic interventions

  • Help run the website in order to reach ASH1L families easily and increase digital footprint

  • Organize ASH1L families meetings

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