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Updated: May 22, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Familiar case of a small TBC1D24 and ATP6V0C -containing microdeletion associated with developmental delay,
Catarina Macedo1, Raquel Rodrigues1, José Paulo Monteiro2
1Serviço de Genética Médica, Departamento de Pediatria, Unidade Local de Saúde de Santa Maria, Lisboa, Portugal.
No abstract available in PubMed .
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