The purpose of this database is to support researchers and clinicians
understand structural changes on alpha-galactosidase A (GLA) caused by Fabry disease mutation

This database contains clinical phenotypes, genotypes, and structures of mutant GLAs.
It is freely accessible and can be reproduced if proper reference is made to the database and its contributions.

This database was constructed and maintained by the research group lead by
H.Sakuraba(department of clinical genetics, Meiji pharmaceutical university.)

(last updated 2021/05/10 ver.3.5)