ALDH3A2 gene mutation

Clinical significance

• ALDH3A2 gene mutations are the cause of Sjoegren-Larsson syndrome

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• aldehyde dehydrogenase 3 family, member A2 (aldehyde dehydrogenase 10, microsomal aldehyde dehydrogenase, ALDH3A2, ALDH10 FALDH)