Normal view MARC view ISBD view

Neuroradiological findings in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency).

Neumaier-Probst, E

Neuroradiological findings in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency). [electronic resource] - Journal of inherited metabolic disease 2004 - 869-76 p. digital

Publication Type: Journal Article; Review

ISSN: 0141-8955

Standard No.: 10.1023/B:BOLI.0000045771.66300.2a doi

Subjects--Topical Terms:
Amino Acid Metabolism, Inborn Errors--pathology
Brain--pathology
Glutarates--urine
Glutaryl-CoA Dehydrogenase
Humans
Infant, Newborn
Magnetic Resonance Imaging
Nervous System Diseases--pathology
Oxidoreductases Acting on CH-CH Group Donors--deficiency

Print
Cite
Add to your cart (remove)
Save record
BIBTEX Dublin Core MARCXML MARC (non-Unicode/MARC-8) MARC (Unicode/UTF-8) MARC (Unicode/UTF-8, Standard) MODS (XML) RIS ISBD
More searches

Search for this title in:
Other Libraries (WorldCat) Other Databases (Google Scholar) Online Stores (Bookfinder.com) Open Library (openlibrary.org)