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Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report
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 Posterior Cor...
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| Publicat a: | BMC Neurol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7802182/ https://ncbi.nlm.nih.gov/pubmed/33435912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-020-02023-5 |
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