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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.
- Source :
- Journal of Inherited Metabolic Disease; Jul2003, Vol. 26 Issue 1, p72-74, 3p
- Publication Year :
- 2003
Details
- Language :
- English
- ISSN :
- 01418955
- Volume :
- 26
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Journal of Inherited Metabolic Disease
- Publication Type :
- Academic Journal
- Accession number :
- 51586019
- Full Text :
- https://doi.org/10.1023/A:1024087832406