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Organ manifestations and long-term outcome of Fabry disease in patients with the GLA haplotype D313Y
OBJECTIVES: The severity of Fabry disease is dependent on the type of mutation in the α-galactosidase A (AgalA) encoding gene (GLA). This study focused on the impact of the GLA haplotype D313Y on long-term organ involvement and function. SETTING AND PARTICIPANTS: In this monocentric study, all parti...
Autores principales: | Oder, Daniel, Üçeyler, Nurcan, Liu, Dan, Hu, Kai, Petritsch, Bernhard, Sommer, Claudia, Ertl, Georg, Wanner, Christoph, Nordbeck, Peter |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838741/ https://www.ncbi.nlm.nih.gov/pubmed/27059467 http://dx.doi.org/10.1136/bmjopen-2015-010422 |
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Correction: Fabry disease due to D313Y and novel GLA mutations
Publicado: (2018)