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Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report

Document Type

Letter

Author

Imarisio, A.; Palmieri, I.; Valente, E.M.; Pilotto, A.; Lupini, A.; Padovani, A.; Biasiotto, G.; Zanella, I.; Currò, R.; Cortese, A.; Vegezzi, E.

Source

In: Parkinsonism and Related Disorders. (Parkinsonism and Related Disorders, June 2024, 123)

Subject

Language

English

ISSN

18735126
13538020

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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