In one clip, a black wolf and a gray wolf slowly crossed a stream in the forest, the water nearly up to their bellies, before ...
LIG4 syndrome is an exceptionally rare disorder caused by a genetic mutation that prevents the body from repairing damaged ...
The gene mutation was isolated in a family in northern Italy where under half of the relations developed the disease. View on euronews ...
Layna Lou Gardiner is an 18-month-old girl who was born with a rare gene mutation on the PBX1 gene that affects almost all of ...
A new case report was published in Volume 16 of Oncotarget on February 5, 2025, titled “Acquired RUFY1-RET rearrangement as a ...
February is American Heart Month, which is an appropriate time to learn how genetic testing can protect your family.
In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches -- gene therapy ...
Limb-girdle muscular dystrophy type 2D (LGMD2D/R3) is a rare genetic disorder caused by mutations in the SGCA gene, leading to defective folding and the loss of functional α-sarcoglycan, with ...