Pages that link to "Q35763202"
Jump to navigation
Jump to search
The following pages link to Increased glycolipid storage produced by the inheritance of a complex intronic haplotype in the α-galactosidase A (GLA) gene. (Q35763202):
Displaying 9 items.
- Inhibition of Intermediate-Conductance Calcium-Activated K Channel (KCa3.1) and Fibroblast Mitogenesis by α-Linolenic Acid and Alterations of Channel Expression in the Lysosomal Storage Disorders, Fabry Disease, and Niemann Pick C (Q37614586) (← links)
- Newborn screening for Fabry disease in the north-west of Spain. (Q41020446) (← links)
- Preliminary Screening Results of Fabry Disease in Kidney Transplantation Patients: A Single-Center Study (Q47816805) (← links)
- Low frequency of Fabry disease in patients with common heart disease (Q49941415) (← links)
- Fabry disease in the Spanish population: observational study with detection of 77 patients (Q52327737) (← links)
- Effectiveness of plasma lyso-Gb3 as a biomarker for selecting high-risk patients with Fabry disease from multispecialty clinics for genetic analysis (Q64046067) (← links)
- Multiple phenotypic domains of Fabry disease and their relevance for establishing genotype- phenotype correlations (Q64060583) (← links)
- Proteostasis regulators modulate proteasomal activity and gene expression to attenuate multiple phenotypes in Fabry disease (Q92399711) (← links)
- Correlation between GLA variants and alpha-Galactosidase A profile in dried blood spot: an observational study in Brazilian patients (Q93036335) (← links)