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Paper Details

Clinical spectrum and genetic causes of mitochondrial hepatopathy phenotype in children.
Hepatol Commun
4
2023
ALF, Chronic, Chronic MH, MH, Patients, RNA, acute liver failure, children, chronic liver disease, enzymatic disorders, liver, mitochondrial DNA, mitochondrial disorder, mitochondrial hepatopathies, mitochondrial hepatopathy, mtDNA, mtDNA depletion, neurodevelopmental delays, nuclear DNA genes, patient, patients
Author NameAffiliation
James E SquiresUPMC Children's Hospital of Pittsburgh
Johan L K Van HoveUniversity of Colorado School of Medicine, Children's Hospital Colorado
Robert H SquiresUPMC Children's Hospital of Pittsburgh
Robert H SquiresUPMC Children's Hospital of Pittsburgh
Simon HorslenUPMC Children's Hospital of Pittsburgh
Estella M AlonsoAnn and Robert H. Lurie Children's Hospital of Chicago
Philip J RosenthalUniversity of California san francisco
Marisa W FriederichUniversity of Colorado School of Medicine, Children's Hospital Colorado
Ronald J SokolUniversity of Colorado School of Medicine, Children's Hospital Colorado
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Release 1.2