Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
Spinocerebellar ataxias (SCAs) constitute a heterogeneous group of more than 40 autosomal-dominant genetic and neurodegenerative diseases characterized by loss of balance and motor coordination due to dysfunction of the cerebellum and its efferent connections. Despite a well-described clinical and pathological phenotype, the molecular and cellular...
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Full title
Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6981692
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6981692
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ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms21010216
