Subject
Genetics (clinical),Genetics
Reference44 articles.
1. American College of Medical Genetics Newborn Screening Expert Group (2006) Newborn screening: toward a uniform screening panel and system. Genet Med 8(Suppl 1):1S–252S
2. Barycki JJ, O’Brien LK, Bratt JM, Zhang R, Sanishvili R, Strauss AW, Banaszak LJ (1999) Biochemical characterization and crystal structure determination of human heart short chain L-3-hydroxyacyl-CoA dehydrogenase provide insights into catalytic mechanism. Biochemistry 38:5786–98
3. Cazorla MR, Verdu A, Perez-Cerda C, Ribes A (2007) Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency. Pediatr Neurol 36:264–7
4. Dubrovsky EB, Dubrovskaya VA, Levinger L, Schiffer S, Marchfelder A (2004) Drosophila RNase Z processes mitochondrial and nuclear pre-tRNA 3′ ends in vivo. Nucleic Acids Res 32:255–62
5. Ensenauer R, Niederhoff H, Ruiter JP, Wanders RJ, Schwab KO, Brandis M, Lehnert W (2002) Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency. Ann Neurol 51:656–9
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