Bookmark
Forward
Explore Literature Results
Explore Clinical Trials Results
QuickView for HS2 (gene)
Most Relevant Literature
- A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin.
- Genetic Analysis and Prenatal Diagnosis of a Family with Hereditary Spherocytosis Caused by a Novel …
- A novel essential splice site variant in SPTB in a large hereditary spherocytosis family.
- Neonatal hereditary spherocytosis caused by a de novo frameshift mutation of the SPTB gene character…
- SPTB related spherocytosis in a three-generation family presenting with kidney failure in adulthood …
Most Relevant Clinical Trials
- Does the Harmonic Scalpel Reduce Blood Loss and OR Time in Major Head and Neck Cancer Surgery Underg…
- Hyoscine Butyl Bromide in Reducing Pain During HSG
- Improved Oral Bioavailability of Curcumin Incorporated Into Micelles
- Evaluation of a Health Monitoring Platform for Elderly in Home Care Context
- Ambulance 'Hypos Can Strike Twice' Study
