DOI:
10.1055/s-00000041
Neuropediatrics
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References
Rüsch CT, Wortmann SB, Kovacs-Nagy R. et al.
Thiamine pyrophosphokinase deficiency due to mutations in the TPK1 gene: a rare treatable neurodegenerative disorder.
Neuropediatrics 2021;
52 (02) 126-132
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