3-Methylglutaconic aciduria in carriers of primary carnitine deficiency.
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| Title: | 3-Methylglutaconic aciduria in carriers of primary carnitine deficiency. |
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| Authors: | Ziats CA; Greenwood Genetic Center, Greenwood, SC, USA; Dell Children's Medical Group, Austin, TX, USA. Electronic address: catherine.ziats@ascension.org., Burns WB; Greenwood Genetic Center, Greenwood, SC, USA., Tedder ML; Greenwood Genetic Center, Greenwood, SC, USA., Pollard L; Greenwood Genetic Center, Greenwood, SC, USA., Wood T; Greenwood Genetic Center, Greenwood, SC, USA; Department of Pediatrics, Section of Genetics and Metabolism, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO, USA., Champaigne NL; Greenwood Genetic Center, Greenwood, SC, USA; Divsion of Genetics, Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA. |
| Source: | European journal of medical genetics [Eur J Med Genet] 2021 Dec; Vol. 64 (12), pp. 104365. Date of Electronic Publication: 2021 Oct 09. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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