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Journal of the American Academy of Dermatology, ISSN 0190-9622, 2011, Volume 67, Issue 2, pp. 269 - 275
Journal Article
Anais Brasileiros de Dermatologia, ISSN 0365-0596, 2014, Volume 89, Issue 1, pp. 141 - 143
Fabry disease is an X-linked, lysosomal storage disease caused by the inherited deficiency of the enzyme α-galactosidase A. The diagnosis is usually late, with... 
Fabry disease | Angiokeratoma | Alpha-galactosidase | Skin Neoplasms - pathology | Fabry Disease - genetics | Humans | Angiokeratoma - pathology | Genotype | Male | Fabry Disease - pathology | Angiokeratoma - genetics | Biopsy | Skin Neoplasms - genetics | Adolescent | Adult | Female | Mutation | Child | Early Diagnosis | Siblings | alpha-Galactosidase | Case Report
Journal Article
ANAIS BRASILEIROS DE DERMATOLOGIA, ISSN 0365-0596, 05/2013, Volume 88, Issue 3, pp. 432 - 437
Journal Article
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