Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...

Scientists have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

A toddler was successfully treated for a rare genetic disease, spinal muscular atrophy, after world-first in-womb therapy.

A new discovery offers hope for Huntington’s disease. This discovery provides hope that a DNA repair process may help slow or ...

Right now, approximately 20 billion red blood cells are busy traveling through your blood vessels. They are delivering oxygen ...

A gene variant identified in a family and studied in a fruit fly model may offer protection against a rare X-linked seizure ...

Sucrase-isomaltase (SI) is an intestinal enzyme critical for the digestion of dietary carbohydrates, particularly sucrose and ...

The mum and dad of a baby with a genetic disease so rare it has no name have vowed to keep fighting for him after the ...

Scientists at the Icahn School of Medicine at Mount Sinai and collaborators have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

A two-and-a-half-year-old girl shows no signs of a rare genetic disorder, after becoming the first person to be treated for ...