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

Author： Mühlhausen C.   Mühlhausen C.   Christensen E.   Schwartz M.   Muschol N.   Ullrich K.   Lukacs Z.  

Publisher： Springer Publishing Company

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.26, Iss.7, 2003-01, pp. : 713-714

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