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Our study revealed a case with dual diagnosis of WBS and NCF1 deficient CGD. The use of NGS has facilitated the elucidation of multiple molecular diagnoses caused by multilocus genomic variations. https://t.co/0MKLFjCXUZ
Our study revealed a case with dual diagnosis of WBS and NCF1 deficient CGD. The use of NGS has facilitated the elucidation of multiple molecular diagnoses caused by multilocus genomic variations. https://t.co/0MKLFjCXUZ
Thank you Frontiers in Immunology for highlighting our study 🙏❤️
New Research: Revealing Chronic Granulomatous Disease in a Patient With Williams-Beuren Syndrome Using Whole Exome Sequencing: Blended phenotypes exhibited by a patient may present a challenge to the establishment of diagnosis. In this study,… https://t.co