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ArticleChild neurology open

Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing.

Christina M Quitmann et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2025
cites it
Full record →Abstract, authors, funding and every citing paper · PMID 34423067