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Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy

Document Type

Article

Author

Berntsson, S.G.; Kristoffersson, A.; Niemelä, V.; Landtblom, A.-M.; Matsson, H.; Casar-Borota, O.; Frykholm, C.; van Duyvenvoorde, H.A.; Richel-van Assenbergh, C.; van der Klift, H.M.

Source

In: Frontiers in Genetics. (Frontiers in Genetics, 2023, 14)

Subject

Language

English

ISSN

16648021

Online Access

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

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