Catalog

Parkinson disease synuclein gene mutation 4q21.23

No MMS code

Link to WHO Definition

Parkinson disease synuclein gene mutation 4q21.23 – http://id.who.int/icd/entity/1729164793

Autosomal Dominant Parkinson Disease due to a mutation in the alpha-synuclein gene on chromosome 4 initially described in a large Italian kindred and in three unrelated families of Greek origin.