ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder. [electronic resource]
Producer: 20160301Description: 186-94 p. digitalISSN:- 1468-6244
- Adult
- Alexander Disease -- genetics
- Child, Preschool
- DNA, Mitochondrial -- genetics
- Exome -- genetics
- Female
- Humans
- Infant
- Iron-Sulfur Proteins -- genetics
- Male
- Middle Aged
- Mitochondrial Diseases -- genetics
- Mutation, Missense
- Neurodegenerative Diseases -- genetics
- Pedigree
- Sequence Analysis, DNA
- White Matter -- abnormalities
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.