Items where Subject is "SBCADD"
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Up a level- CSHL Subject List (1)
- diseases & disorders (1)
- congenital hereditary genetic diseases (1)
- SBCADD (1)
- congenital hereditary genetic diseases (1)
- diseases & disorders (1)
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M
Madsen, P. P., Kibæk, M., Roca, X., Sachidanandam, R., Krainer, A. R., Christensen, E., Steiner, R. D., Gibson, K. M., Corydon, T. J., Knudsen, I., Wanders, R. J. A., Ruiter, J. P. N., Gregersen, N., Andresen, B. S. (2006) Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping. Human Genetics, 118 (6). pp. 680-690. ISSN 03406717