This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the MYH3 gene.
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Clinicals who identify a patient with a mutation in MYH3 are invited to submit clinical and molecular information to the database.
Anna Hakonen, MD, PhD, Helsinki University Hospital (HUS) and University of Turku, Helsinki, Finland, anna.hakonen@hus.fi