论文信息 - Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition - 字舞流文

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

F. Bernier | J. Parboosingh | P. Bridge | A. Chan | A. Chan | R. Casey | P. Ferreira | F. Snyder | D. R. Mcleod | K. Davey | Casey | Robin