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

Open access

Research article

First published 2021

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

Christina M. Quitmann, Stephan Rust, Janine Reunert [...]

Child Neurology Open

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