Isobutyryl-CoA dehydrogenase deficiency: isobutyrylglycinuria and ACAD8 gene mutations in two infants
Document Type: | Article |
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Language: | English |
Author: | J. O. Sass, S. Sander, J. Zschocke |
Parent Title (English): | Journal of Inherited Metabolic Disease |
Volume: | 27 |
Issue: | 6 |
First Page: | 741 |
Last Page: | 745 |
ISSN: | 0141-8955 |
DOI: | https://doi.org/10.1023/B:BOLI.0000045798.12425.1b |
PMID: | https://pubmed.ncbi.nlm.nih.gov/15505379 |
Publisher: | Kluwer Academic Publishers |
Place of publication: | Dordrecht |
Date of first publication: | 2004/11/01 |
Departments, institutes and facilities: | Institut für funktionale Gen-Analytik (IFGA) |
Dewey Decimal Classification (DDC): | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Entry in this database: | 2018/08/18 |