Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease

Genetics in Medicine - Tập 8 - Trang 346-353 - 2006
Natalie Jansen Street1,2,3, Michael S. Yi4,5, Laurie A. Bailey1, Robert J. Hopkin1,5
1From the Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;
2College of Allied Health Sciences, University of Cincinnati, Cincinnati, OH;
3Currently affiliated with the Division of Human Development and Disability, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA.
4Department of Internal Medicine, University of Cincinnati, Cincinnati, OH
5Department of Pediatrics, University of Cincinnati, Cincinnati, OH;

Tài liệu tham khảo

Desnick, 2001, α -Galactosidase A deficiency: Fabry disease, The metabolic bases of inherited disease. 8th ed, 3733 Gold Miners Deegan Gupta Mehta MacDermot Kampmann Whybra Hays Hays Vickrey Rupp Samsa Hoffmann Eng Ries Baehner Alvarez-Ude Schiffmann Desnick MacDermot
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Thông tin xuất bản

Genetics in Medicine

Tập 8

346-353

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