A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy.

Added 888 days ago (17.04.2017)
Authors: Jackson CB, Hahn D, Schröter B, Richter U, Battersby B, Schmitt-Mechelke T, Martinen P, Nuoffer JM, Schaller A
PubMed id: 28412374
Read article