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GBA1 Apart from the abovementioned gene mutations, mutations of the GBA1 gene, which encodes GCase, a lysosomal enzyme that hydrolyzes glucosylceramide to glucose and ceramide, are among the most common genetic risk factors for the development of PD [17]

For example, these shots are often used to prevent or treat pernicious anemia a rare blood disorder that results from the intestines not absorbing enough B12

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