Enzyme replacement reverses abnormal cerebrovascular responses in Fabry disease

作者: David F Moore , Gheona Altarescu , Peter Herscovitch , Raphael Schiffmann

DOI: 10.1186/1471-2377-2-4

关键词:

摘要: Background Fabry disease is a lysosomal X-linked enzyme deficiency of α-galactosidase A associated with an increased mortality and morbidity due to renal failure, cardiac early onset stroke.

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