Swedish and Tyrolean researchers have succeeded in deciphering the molecular structure of the neurofibromin with extremely high accuracy
The basics in brief
- Researchers have deciphered the molecular structure of the neurofibrillary fibril.
- This advances research in hereditary neurofibromatosis.
Scientists from the Medical University of Innsbruck and Stockholm University have deciphered the molecular structure of the neurofibromin with high accuracy. « Results bring search in hereditary neurofibromatosis A big step forward,” wrote Jane Ebe Innsbruck.
“Patients with neurofibromatosis present with a variety of symptoms, often caused by benign or malignant skin tumors and from the nervous systemIt can occur as early as infancy,” explained structural biologist Bernhard Robb.
“With a birth rate of 1:3,000, neurofibromatosis is one of the most common genetic diseases, and an understanding of molecular mechanisms This disease is a prerequisite for the development of therapeutic methods and active components, ”writes the scientist.
“Alcohol buff. Troublemaker. Introvert. Student. Social media lover. Web ninja. Bacon fan. Reader.”
More Stories
How is it treated and how can it be prevented?
Behavioral scientist: Curiosity enhances biodiversity
Science: Microplastics from ships and the sea: investigation in the North Sea