PMID 27301544 2016 DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
PMID 29899447 2018 Structural basis of mitochondrial receptor binding and constriction by DRP1.
PMID 26992161 2016 Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
PMID 27328748 2016 Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy.
PMID 27145208 2016 A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
PMID 27301544 2016 DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
PMID 27328748 2016 Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy.
PMID 29899447 2018 Structural basis of mitochondrial receptor binding and constriction by DRP1.
PMID 27145208 2016 A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
PMID 17460227 2007 A lethal defect of mitochondrial and peroxisomal fission.