Mitochondrion

Mitochondrion Journal

Publication venue for

SPATA5 mutations identified by whole exome sequencing cause a novel autosomal recessive defect of mitochondrial morphogenesis characterized by microcephaly, intellectual disability, seizures, and hearing loss. 31:101-102. 2016
Hepatic cirrhosis & neurological deficits in a male with de novo heteroplasmic mitochondrial DNA mutation. 13:938-938. 2013
Diagnosis and treatment of secondary mitochondrial disease. 12:563-564. 2012

International Standard Serial Number (ISSN)

1567-7249