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Asparagine Synthetase Deficiency clinical trials

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NCT ID: NCT03587155 Recruiting - Clinical trials for Genetic Diseases, Inborn

Study on the Mechanism of Neurodevelopment Dysplasia of Fetal Brain Caused by ASNS Gene Mutation

Start date: October 28, 2017
Phase:
Study type: Observational

The investigators propose to analyze a brain sample and/or peripheral blood by single cell RNA seq from aborted embryos with ASNS mutation.