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phenylketonuria (1)
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When one disease is not enough: Succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency due to a novel mutation in OXCT1 in an infant with known phenylketonuria
(2017)
Schwade, Jan-Niclas
;
Endmann, Matthias
;
Hofmann, Thomas
;
Rust, Stephan
;
Sass, Jörn Oliver
;
Rutsch, Frank
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