Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
Abstract Background Glucocerebrosidase (GBA) heterozygous variants are the most important genetic risk factor for the development of alpha-synucleinopathies (i.e., Parkinson’s disease and Dementia with Lewy Bodies). Herein, we report for the first time on a patient with a clinical diagnosis of Poste...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMC
2021-01-01
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| Serie: | BMC Neurology |
| Soggetti: | |
| Accesso online: | https://doi.org/10.1186/s12883-020-02023-5 |
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