Assignment of the Human Mitochondrial Very-Long-Chain Acyl-CoA Dehydrogenase Gene (LCACD) to 17p13 byin SituHybridization
Author:
Publisher
Elsevier BV
Subject
Genetics
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype;Clinica Chimica Acta;2001-10
2. Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency;Pediatric Neurology;2000-02
3. THE MOLECULAR DIAGNOSIS OF METABOLIC MYOPATHIES;Neurologic Clinics;2000-02
4. Chromosomal locations of the mouse fatty acid oxidation genes Cpt1a, Cpt1b, Cpt2, Acadvl, and metabolically related Crat gene;Mammalian Genome;1998-08-01
5. Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency;Human Molecular Genetics;1997-08-01
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