This website provides information on patients with mutations in the MYH3 gene, including clinical data, molecular data, management and research options.

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.

Choose page:

• MYH3 autosomal recessive
• MYH3 autosomal dominant

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