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Rare Disease Day 2020

It was our honor to attend the first-ever gathering of KDM5C families at the Rare Disease Day 2020 event at Albert Einstein College of Medicine in New York. Families from the US and Europe connected with each other and with the research community. Iwase lab alumna Christina Vallianatos (PhD 2019) spoke as an event panelist to share KDM5C information. Thanks to our colleagues in the Secombe lab for organizing, and many thanks to the families for attending! You inspire our work to uncover the basis of KDM5C and MRXSCJ syndrome!













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KDM5C Registry is now live

In our effort to better understand KDM5C-related disorder, we created the KDM5C Registry: https://redcap.link/KDM5C-registry Our mission is to improve the lives of children, young adults, and families

The University of Michigan Medical School

Human Genetics Department

©2018 by Chromatin Neurobiology Lab. 

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