Compound heterozygosity in the glutaryl‐CoA dehydrogenase gene with R227P mutation in one allele is associated with no or very low free glutarate excretion
- 1 July 1997
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 20 (3), 383-386
- https://doi.org/10.1023/a:1005390214391
Abstract
No abstract availableKeywords
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