Scientists from a collaboration of Australian research institutions have proposed that editing multiple genetic variants in ...

The gene mutation was isolated in a family in northern Italy where under half of the relations developed the disease. View on ...

Study highlights use of techniques such as long-read genome sequencing, optical genome mapping, and RNA sequencing for rare ...

Scientists are unraveling the mystery of what triggers Huntington's disease, a devastating hereditary disorder that strikes ...

Study explains long-standing question of why Huntington’s disease symptoms typically do not appear until midlife even though ...

A new mega-database of half a million mutations may flag new ways of treating genetic disease, scientists say.

More Than 40 Adult Sickle Cell Disease Patients Now Enrolled in BEACON Trial of BEAM-101; Beam Expects to Dose 30 Patients ...

Researchers at Tufts University revealed a possible molecular mechanism explaining how the DNA repeats are broken and then expanded in the Huntington’s disease gene, pointing to a component of the ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate ...

People genetically susceptible to Huntington's disease often see their movement, mood, and cognition decline slowly over time.