Cite
HARVARD Citation
Quitmann, C. et al. (2021). Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing. Child neurology open. p. . [Online].
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Quitmann, C. et al. (2021). Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing. Child neurology open. p. . [Online].