Header

UZH-Logo

Maintenance Infos

Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding Delta1-pyrroline-5-carboxylate synthase


Baumgartner, M R (2000). Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding Delta1-pyrroline-5-carboxylate synthase. Human Molecular Genetics, 9(19):2853-2858.

Statistics

Citations

Dimensions.ai Metrics

Altmetrics

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:2000
Deposited On:04 Feb 2020 13:40
Last Modified:31 Jul 2020 03:45
Publisher:Oxford University Press
ISSN:0964-6906
OA Status:Closed
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1093/hmg/9.19.2853

Download

Full text not available from this repository.
View at publisher

Get full-text in a library