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Disease manifestations and X inactivation in heterozygous females with Fabry disease

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Year: 2006
Type: article
Study design: Observational Study
Source: Acta Paediatrica
DOI: 10.1080/08035320600618809
Authors: Esther Maier, Stephanie Osterrieder, Catharina Whybra, Markus Ries, Andreas Gal, Michael Beck, Adelbert Roscher, Ania Muntau
Institutions: Ludwig-Maximilians-Universität München, Johannes Gutenberg University Mainz, National Institutes of Health, University Medical Center Hamburg-Eppendorf
Language: English

Topic: Lysosomal Storage Disorders Research
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W2045708809
FWCI: 3.921
Cites: 59
Cited by: 115
Related to: 10
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