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1. Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: a novel mutation in a Turkish patient with glutaric aciduria type I.

   1. Mühlhausen, C
   2. Christensen, E
   3. Schwartz, M
   4. Muschol, N
   5. Ullrich, K
   6. Lukacs, Z

   2003 - Forschungsinformationssystem des UKE