Drögemöller Lab
Drögemöller Lab
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Farhad Karbassi
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Bi-allelic GOT2 mutations cause a treatable malate-aspartate shuttle-related encephalopathy
Glutaminase deficiency caused by short tandem repeat expansion in GLS
Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function
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