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Fabry Disease and Early Stroke
Fabry disease, an X-linked lysosomal storage disorder, results from deficient activity of the enzyme α-galactosidase A. Affected males with the classic phoenotype have acroparaesthesias, hypohidrosis, and corneal opacities in childhood and develop renal failure, cardiac hypertrophy or strokes in the...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE-Hindawi Access to Research
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3138050/ https://ncbi.nlm.nih.gov/pubmed/21776363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4061/2011/615218 |
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