DOI:
10.1055/s-00000041
Neuropediatrics
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References
Zhu L, Wu R, Ye Z. et al.
Identification of two novel TPK1 gene mutations in a Chinese patient with thiamine pyrophosphokinase deficiency undergoing whole exome sequencing.
J Pediatr Endocrinol Metab 2019;
32 (03) 295-300
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