Hydroxymethylbilane Synthase: Complete Genomic Sequence and Amplifiable Polymorphisms in the Human Gene
Han‐Wook Yoo(CHA University Bundang Medical Center), Robert J. Desnick(Icahn School of Medicine at Mount Sinai), Cecilia A. Warner(Icahn School of Medicine at Mount Sinai), Chia‐Hsiang Chen(Center for HIV and Hepatogastroenterology)
Cited by 100
Related Papers
Agalsidase-Beta Therapy for Advanced Fabry Disease
|Annals of Internal Medicine|2007|565
Acid sphingomyelinase deficient mice: a model of types A and B Niemann–Pick disease
|Nature Genetics|1995|477
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
|Science Translational Medicine|2018|411
Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy
|Nephrology Dialysis Transplantation|2009|366
Ten-year outcome of enzyme replacement therapy with agalsidase beta in patients with Fabry disease
|Journal of Medical Genetics|2015|363