New study looks at DNMT3A mosaicism
Dr. Ayala Tovy, a researcher at Baylor College of Medicine and a medical advisory board member of The TBRS Community, and her colleagues have described
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Dr. Ayala Tovy, a researcher at Baylor College of Medicine and a medical advisory board member of The TBRS Community, and her colleagues have described
The British Society for Genetic Medicine and the Clinical Genetics Society have developed an online tool to help determine the risks of COVID-19 for adults with rare
The CoIN study is looking into how the coronavirus pandemic is affecting the lives of children with rare diseases living in the UK. The researchers are seeking
The Rare Diseases Clinical Research Network, which is funded by the US National Institutes of Health, is gathering information from individuals with rare diseases or
The National Organization for Rare Disorders (NORD) has welcomed The TBRS Community as a member, joining 300 other patient organizations. NORD is a leading advocacy group for
Researchers at the University of California, Riverside, have examined the function of a particular mutation in the DNMT3A gene called R882H. This variant is a common driver