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Neurodevelopmental disorder in a patient with HMBS and SCN3A variants-A possibly blended phenotype further delineating autosomal recessive HMBS related disease

Document Type

Journal

Author

Klaniewska, M.; Rydzanicz, M.; Bladowska, J.; Borys-Iwanicka, A.; Iwanicka-Pronicka, K.; Wasilewski, R.; Odnoczko, E.; Zubkiewicz-Kucharska, A.; Smigiel, R.; Ploski, R.

Source

AMERICAN JOURNAL OF MEDICAL GENETICS PART A; APR 3 2024, 8p.

Subject

Language

English

ISSN

15524833

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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