SLC24A4 gene

IMPORTANCE Recent large-scale genome-wide association studies have discovered several genetic variants associated with Alzheimer… (More)

Defects in WDR72 (WD repeat-containing protein 72) cause autosomal recessive hypomaturation amelogenesis imperfecta. We generated… (More)

OBJECTIVE To investigate the top late-onset Alzheimer disease (LOAD) risk loci detected or confirmed by the International… (More)

Ameloblasts express transmembrane proteins for transport of mineral ions and regulation of pH in the enamel space. Two major… (More)

Amelogenesis imperfecta is a heterogeneous group of genetic conditions affecting enamel formation. Recently, mutations in solute… (More)

Calcium ions in the uterine endometrium are essential for the establishment and maintenance of pregnancy, but the cellular and… (More)

A combination of autozygosity mapping and exome sequencing identified a null mutation in SLC24A4 in a family with hypomineralized… (More)

Sixteen nuclear magnetic resonance (NMR) spectroscopy lipoprotein measurements of more than 1,000 subjects of GOLDN study, at… (More)

Despite the recent rapid growth in genome-wide data, much of human variation remains entirely unexplained. A significant… (More)

The evidence for the existence of genetic susceptibility variants for the common form of hypertension ("essential hypertension… (More)