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Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review

Document Type

Article

Author

Bi, S.; Dai, L.; Liu, G.; Jiang, L.; Wang, L.; Teng, M.; Teng, R.-J.

Source

In: Frontiers in Genetics. (Frontiers in Genetics, 13 January 2023, 13)

Subject

Language

English

ISSN

16648021

Online Access

Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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