My father was a folk song collector, and I grew up listening to the music of Woody Guthrie. On July 14th, folk music enthusiasts will be celebrating the 105th anniversary of Guthrie’s birth in his hometown of Okemah, OK. Besides being renowned for writing “This Land is Your Land” and other folk classics, Guthrie has another more tragic claim to fame: he provided the world with a glimpse at the devastation caused by a rare, inherited neurological disorder called Huntington’s disease.
When Guthrie died from complications of Huntington’s a half-century ago, the disease was untreatable. Sadly, it still is. But years of basic science advances, combined with the promise of innovative gene editing systems such as CRISPR/Cas9, are providing renewed hope that we will someday be able to treat or even cure Huntington’s disease, along with many other inherited disorders.
Tags: adult neurons, brain, CAG, CRISPR/Cas9, gene editing, genetics, genomics, HTT gene, huntingtin, Huntington's disease, inherited disease, misfolded proteins, muscular dystrophy, mutation, neurodegenerative disorders, neurological disorders, neuron, rare disease, sickle cell disease, striatum