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

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Bibliographic Details
Title: Tubulin Folding Cofactor D Deficiency: Missing the Diagnosis With Whole Exome Sequencing.
Authors: Quitmann, Christina M., Rust, Stephan, Reunert, Janine, Biskup, Saskia, Fiedler, Barbara, Marquardt, Thorsten
Source: Child neurology open 1/1/2021.
Journal Info: Publisher: Sage Publications Inc. ISSN: 2329-048X
Database: MEDLINE Ultimate
Description
ISSN:2329-048X
DOI:10.1177/2329048X211034969