1. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition. Issue 5 (31st July 2005) Authors: Davey, K M; Parboosingh, J S; McLeod, D R; Chan, A; Casey, R; Ferreira, P; Snyder, F F; Bridge, P J; Bernier, F P Journal: Journal of medical genetics Issue: Volume 43:Issue 5(2006) Page Start: 385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗