A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene.
Fragaki, Konstantina
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene. [electronic resource] - Mitochondrion Sep 2009 - 346-52 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1872-8278
10.1016/j.mito.2009.06.002 doi
Adult
Child
Cytochromes b--deficiency
DNA, Mitochondrial--genetics
Humans
Infant, Newborn
Male
Mitochondrial Diseases--genetics
Multiple Organ Failure--genetics
Mutation, Missense
Point Mutation
Young Adult
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene. [electronic resource] - Mitochondrion Sep 2009 - 346-52 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
1872-8278
10.1016/j.mito.2009.06.002 doi
Adult
Child
Cytochromes b--deficiency
DNA, Mitochondrial--genetics
Humans
Infant, Newborn
Male
Mitochondrial Diseases--genetics
Multiple Organ Failure--genetics
Mutation, Missense
Point Mutation
Young Adult