SCN8A gene
The SCN8A gene is one of many genes that are associated with epilepsy and other related disorders. Mutations in this gene can…
Aromatic l-amino acid decarboxylase deficiency
Aromatic l-amino acid decarboxylase deficiency is a rare genetic condition caused by a deficiency in the enzyme aromatic l-amino acid decarboxylase. This…
PNKD gene
Pnkd gene is a gene responsible for the development of the paroxysmal nonkinesigenic dyskinesia (PNKD), a neurological disorder characterized by involuntary movements.…
Chromosome 18
The term “chromosome 18” refers to one of the 23 pairs of chromosomes in the human genome. Chromosomes are the molecular structures…
Skin Cancer Screening
Skin cancers are one of the most common types of cancers worldwide. Detecting them early is crucial for maintaining good health. Regular…
TFAP2B gene
The TFAP2B gene is a key regulator of gene expression and plays a crucial role in various biological processes. It is involved…
ITGB3 gene
The ITGB3 gene is a gene that is only found in humans. It is located within the Glanzmann thrombasthenia (GT) blood clotting…
Chromosome 19
Chromosome 19 is one of the 23 pairs of chromosomes in humans. It is a relatively small chromosome, spanning about 58 million…
PCSK9 gene
The PCSK9 gene is a genetic variant that plays a crucial role in the regulation of cholesterol levels in the bloodstream. It…