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- [3] Severe Clinical and Neurological manifestations in an Indian Glutaric Acidemia type I patient due to a novel mutation in the Glutaryl-CoA dehydrogenase gene RESEARCH JOURNAL OF BIOTECHNOLOGY, 2020, 15 (04): : 82 - 85
- [4] A novel mutation in the glutaryl-CoA dehydrogenase gene (GCDH) in an Iranian patient affected with Glutaric acidemia type 1 CLINICAL CASE REPORTS, 2021, 9 (09):